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Journal articles on the topic 'Opitz'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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1

Opitz, Weston. "Taxonomy of the New World Pseudichnea complex (Coleoptera: Cleridae: Peloniinae)." Canadian Entomologist 148, no. 3 (January 7, 2016): 260–83. http://dx.doi.org/10.4039/tce.2015.60.

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AbstractThe Pseudichnea complex involves the genera Ambitus, new genus, Ampleris, new genus, Sirpa, new genus, and Pseudichnea Schenkling. Ambitus includes one species, A. anticus Opitz, new species. Ampleris includes A. achira Opitz, new species, A. angustata Opitz, new species, A. cava Opitz, new species, A. orosi Opitz, new species, A. primitura Opitz, new species,A. rufocapilla Opitz, new species, and A. buenavista Opitz, new species.Pseudichnea includes P. acia Opitz, new species, P. arima Opitz, new species, P. eliminata Schenkling, and P. gracila Opitz, new species. Sirpa includes S. cauda Opitz, new species, S. flavoapiculis Opitz, new species, and S. skelleyi Opitz, new species. Morphological observations, particularly those based on mouthpart structure, suggest that these beetles are predatory. Their leg construction, especially development of the tarsal pads and ungues, suggest that they are lignicolous beetles that inhabit the woody components of arboreal vegetation, a niche in which they presumably pursue bark-beetle prey. Besides descriptions, this treatise includes a key to genera and species, 72 line drawings, eight electron micrographs, 16 habitus illustrations, and two distribution maps.

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2

OPITZ, WESTON. "Classification, natural history, and evolution of Epiphloeinae (Coleoptera: Cleridae). Part VII. The genera Hapsidopteris Opitz, Iontoclerus Opitz, Katamyurus Opitz, Megatrachys Opitz, Opitzia Nemesio, Pennasolis Opitz, new genus, Pericales Opitz, new genus, Pteroferus Opitz, new genus, and Turbophloeus Opitz, new genus." Zootaxa 1754, no. 1 (April 21, 2008): 1. http://dx.doi.org/10.11646/zootaxa.1754.1.1.

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This study deals with minimally speciose epiphloeine genera. Hapsidopteris, based on H. diastenus Opitz, (type locality: México: Jalapa), is the presumed sister taxon of Opitzia Nemésio [type species: O. chiapas (Opitz), type locality: México: Chiapas: 39 km NW Comitán] a bitypic genus that also includes O. apicula, new species (type locality: Bolivia: Santa Cruz: Amboro Road, above Achira Campo). Two species define Iontoclerus Opitz, I. humeralis (Klug) (type locality: Brazil: Parà) and I. sericeus (Klug) (type locality: Brazil: Rondonia: 62 km SE Ariquemes), whose presumed sister genus is the monotypic Pericales, new genus, based on P. albogilvus, new species (type locality: Haiti: Sud-Ouest: Massif de La Selle, Morne d’Enfer). The Middle American bitypic Katamyurus Opitz [type species: K. paxillus Opitz, type locality: Nicaragua: Cerro Chimborazo], which also includes K. albopaniculus, new species (type locality: México: Sinaloa: 14 km NE La Cap. del Taxte), is considered the sister taxon to Ellipotoma Spinola (type species: E. tenuiformis Spinola. Type locality: Colombia). Megatrachys Opitz (type species: Megatrachys paniculus Opitz (type locality: México: Chiapas: 8 km W San Cristóbal) contains two additional species, M. bibara, new species (type locality: Guatemala: Zacapa: 2 km San Lorenzo) and M. truncatia, new species (type locality: México: Chiapas: 47.5 km NW Comitán) and is the hypothesized sister taxon to Pennasolis, new genus [type species; P. merkeli (Horn), type locality: Arizona: Cochise County, South West Research Station, 8 km W Portal], which in addition to the type species also contains P. californica (Van Dyke) (type locality: California: Yosemite National Park, Yosemite Valley. The phylogenetic relationships of two South American monotypic genera have not been deciphered; these are Pteroferus, new genus, based on P. zolnerowichi, new species (type locality: Brazil: Santa Catarina: Nova Teutonia), and Turbophloeus, new genus, based on T. simplex (Schenkling) whose type locality is Bolivia: Santa Cruz: Amboro National Park, Los Volcanes. Lectotypes are designated for Pennasolis merkeli (Horn), Iontoclerus humeralis (Klug), I. sericeus (Klug), and Turbophloeus simplex (Schenkling). The latter binomial represents a new combination whose specific epithet was originally associated with Epiphloeus.

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3

Conlon, Brendan J., and Tadhg O'Dwyer. "The G syndrome/Opitz oculo-genital-laryngeal syndrome/Opitz BBB/G syndrome/Opitz-Frias syndrome." Journal of Laryngology & Otology 109, no. 3 (March 1995): 244–46. http://dx.doi.org/10.1017/s0022215100129810.

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AbstractWe report on a family exhibiting a range of congenital anomalies consistent with the G syndrome of Opitz. Three members of the family had laryngo-tracheo-oesophageal clefts, one of which succumbed. There was a strong family history of perinatal mortality on the maternal side of the family. We note also the paucity of reported cases of this syndrome in the otolaryngological literature and stress the necessity of early diagnosis in the management.

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4

Choudhary, Ramesh, Romesh Gauttam, Vishnu Pansari, and Anand Kumawat. "Variant of bohring-opitz syndrome: A rare case report." IP Journal of Paediatrics and Nursing Science 4, no. 2 (July 15, 2021): 84–86. http://dx.doi.org/10.18231/j.ijpns.2021.017.

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Bohring–Opitz syndrome also known as Opitz C syndrome or Oberklaid–Danks syndrome is a rare syndrome. We are reporting a 2 months old male child with Bohring-Opitz like syndrome with all classical features and eventration of diaphragm (left side) which has not been reported yet with this syndrome. To our knowledge, a total of 23 cases with this syndrome have been reported in the medical literature to date and this is probably the first case report from India. Although there is overlap, a clinical distinction from the Bohring-Opitz syndrome and other syndromes seems possible, and thus a specific causal entity may be postulated.

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5

Opitz, Weston. "Taxonomy of the New World checkered beetle genus Akonesis Opitz (Coleoptera: Cleridae: Peloniinae)." Canadian Entomologist 150, no. 2 (January 31, 2018): 141–55. http://dx.doi.org/10.4039/tce.2017.67.

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AbstractThe genera Akonesis Opitz, Crusbatus Opitz, and Diutius Opitz, which comprise a monophyletic group within Peloniinae (Coleoptera: Cleridae), are discussed. The species of Akonesis are reviewed. There are five recognised species of Akonesis: A. pictipennis (Gorham), A. privoatus Opitz new species, A. ridens (Gorham), A. strictus Opitz new species, and A. vittatus (Spinola). According to the morphological analysis performed herein, the species treated in this work are thought to be predatory. Colour patterns of the elytra and field observations suggest that members of Akonesis and Diutius are involved in Batesian mimicry with Chrysomelidae (Coleoptera), and in particular with Galerucinae. Included in this treatise are: a brief discussion of the natural history and evolution of Akonesis species, one Bootstrap consensus tree, a key to Akonesis species, a phylogenetic tree generated by WINCLADA in conjunction with NONA, 15 line drawings, 10 electron micrographs, one distribution map, four photographs of male terminalia, and five colour habitus photographs.

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6

Castrillo de Larreta-Azelain, María Dolores, and Marina Sanfilippo. "La Dafne de Rinuccini y la de Opitz: el comienzo de la ópera italiana y alemana. Edición bilingüe." Epos : Revista de filología, no. 29 (January 1, 2013): 403. http://dx.doi.org/10.5944/epos.29.2013.15202.

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7

Crawford, Doreen, and Annette Dearmun. "Opitz-Frias syndrome." Nursing Children and Young People 29, no. 10 (December 5, 2017): 20. http://dx.doi.org/10.7748/ncyp.29.10.20.s24.

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8

BOLSIN, S. N., and C. GILLBE. "Opitz-Frias syndrome." Anaesthesia 40, no. 12 (December 1985): 1189–93. http://dx.doi.org/10.1111/j.1365-2044.1985.tb10657.x.

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9

Neri, Giovanni, and Marco Cappa. "The Opitz syndrome." American Journal of Medical Genetics 30, no. 3 (July 1988): 851. http://dx.doi.org/10.1002/ajmg.1320300323.

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10

Haaf, Thomas, Renate Hofmann, and Michael Schmid. "Opitz trigonocephaly syndrome." American Journal of Medical Genetics 40, no. 4 (September 15, 1991): 444–46. http://dx.doi.org/10.1002/ajmg.1320400413.

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11

Sedano, Heddie O., Robert J. Gorlin, and John M. Opitz. "Opitz Oculo-Genital-Laryngeal syndrome (Opitz BBB/G compound syndrome)." American Journal of Medical Genetics 30, no. 3 (July 1988): 847–49. http://dx.doi.org/10.1002/ajmg.1320300322.

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12

Dunphy, Graeme. "Martin Opitz und die Mittelalterlichen Alexandergeschichten." Daphnis 31, no. 1-2 (November 23, 2002): 299–316. http://dx.doi.org/10.1163/18796583-0310102012.

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Dieser Artikel beschäftigt sich mit der Rezeption des Mittelalters in der Barockzeit am Beispiel von Martin Opitz und den mittelalterlichen Alexandererzählungen. Im Apparat zu seiner Annolied-Ausgabe läßt sich Opitz auf einen längeren Diskurs über den Alexanderstoff ein, wie dieser in mehreren mittelalterlichen Werken vorkommt. Neben dem Annolied selbst stellt er hier vor allem die Kosmographie des Aethicus von Istrien und ein anonymes Werk mit dem Titel Excerptum de vita Alexandri Magni zur Diskussion. Damit beeinflußt er nachhaltig die wissenschaftliche Rezeption von Aethicus in den darauffolgenden Jahrhunderten. Der Artikel untersucht diese Konstellation und bietet nebenbei einige neuen Einsichten zum Briefwechsel von Opitz mit seinem wichtigsten Gewährsmann, Claude Saumaise.

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13

Dalben, Gisele da Silva, Daniela Gamba Garib, Rayane de Oliveira Pinto, Antonio Richieri-Costa, and Luís Antônio de Assis Taveira. "Craniofacial Morphology in Patients With Opitz G/BBB Syndrome." Cleft Palate-Craniofacial Journal 56, no. 10 (June 19, 2019): 1366–72. http://dx.doi.org/10.1177/1055665619857001.

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Objective: To compare the cephalometric characteristics of patients with and without Opitz G/BBB syndrome type I. Design: Cross-sectional, case–control study. Setting: Tertiary cleft center in Brazil. Participants: Eighteen individuals with Opitz G/BBB syndrome with complete bilateral cleft lip and palate (BCLP), compared to 18 individuals with nonsyndromic complete cleft lip and palate and 18 individuals without malformations, matched for gender and age. Interventions: Pretreatment lateral cephalograms of all patients were manually traced and digitized for achievement of linear and angular measurements. Main Outcome Measures: Analysis of variance or Kruskal-Wallis followed by Tukey tests were used for intergroup comparisons at a significance level of P < .05. Results: Individuals with Opitz G/BBB syndrome exhibited alterations in SNGn, P-Co, and N’-Pr/Po-Or that were not attributable to BCLP. Co-Go, Sella-Nasion-Supramentale, ANB (maxillo-mandibular relationship), and anterior nasal spine-posterior nasal spine (ANS-PNS)/U1A-U1T were significantly different in both G/BBB and BCLP groups compared to control, but not different between G/BBB and BCLP groups. Anterior nasal spine-posterior nasal spine/Go-Gn, ANS-PNS, V-Upper pharyngeal wall, and U-lower pharyngeal wall were different in nonsyndromic BLCP compared to nonsyndromic controls and Opitz G/BBB group. Conclusion: Patients with Opitz G/BBB syndrome exhibited some unique cephalometric alterations compared to patients with nonsyndromic complete BCLP and controls.

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14

Nakane, Takaya, Takeo Kubota, Yoshimitsu Fukushima, Yukiko Hata, Junko Ishii, and Atsushi Komiyama. "Opitz trigonocephaly (C)-like syndrome, or Bohring-Opitz syndrome: Another example." American Journal of Medical Genetics 92, no. 5 (2000): 361–62. http://dx.doi.org/10.1002/1096-8628(20000619)92:5<361::aid-ajmg13>3.0.co;2-e.

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15

Mourey, Marie-Thérèse. "Historizität und Fiktion in Martin Opitzens Versepen." Daphnis 47, no. 1-2 (March 5, 2019): 221–37. http://dx.doi.org/10.1163/18796583-04701008.

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This article seeks to shed new light on well known epic poems by Martin Opitz, especially the Trostgedichte, which were written at the beginning of the war. The relationship between history and fiction is developed through a specific kind of “story telling”, which aims at presenting the protestants as victims of persecution within all Europe, without mentioning the origins and reasons of this specific war in Germany. The author Martin Opitz, as their harbinger, tries to give moral and philosophical support to his readers but also calls for a strong resistance. The different epic works Opitz wrote during his short life can thus be seen as a encrypted and steadily updated comment to the current political and military events.

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16

Demirdöven, Mehmet, Hamza Yazgan, Mevlit Korkmaz, Arzu Gebeşçe, and Alparslan Tonbul. "Smith-Lemli-Opitz Syndrome: A Case with Annular Pancreas." Case Reports in Pediatrics 2014 (2014): 1–3. http://dx.doi.org/10.1155/2014/623926.

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Smith-Lemli-Opitz syndrome is an autosomal recessive disease of cholesterol metabolism. It is a multiple malformation syndrome with typical dysmorphic features such as bitemporal narrowing, ptosis, epicanthus, microcephaly, micrognathia, and cardiovascular, skeletal, urogenital, and gastrointestinal anomalies. This report presents a typical case of Smith-Lemli-Opitz syndrome with annular pancreas which is an unreported gastrointestinal abnormality.

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17

Millichap, J. Gordon. "Smith-Lemli-Opitz Syndrome." Pediatric Neurology Briefs 10, no. 9 (September 1, 1996): 71. http://dx.doi.org/10.15844/pedneurbriefs-10-9-11.

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18

Millichap, J. Gordon. "Smith-Lemli-Opitz Syndrome." Pediatric Neurology Briefs 12, no. 9 (September 1, 1998): 65. http://dx.doi.org/10.15844/pedneurbriefs-12-9-1.

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19

LILLBACK, PETER A. "INTERVIEW WITH PETER OPITZ." CURRENT DEBATES IN REFORMED THEOLOGY: PRACTICE 4, no. 2 (October 22, 2018): 225–32. http://dx.doi.org/10.35285/ucc4.2.2018.int.

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20

Shah, Ira, Alpana Ohri, Rachana Gedam, and Uma Ali. "Smith-Lemli-Opitz-syndrome." Indian Journal of Human Genetics 18, no. 2 (2012): 235. http://dx.doi.org/10.4103/0971-6866.100779.

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21

Smithells, R. W. "SMITH-LEMLI-OPITZ SYNDROME." Developmental Medicine & Child Neurology 10, no. 5 (November 12, 2008): 663–65. http://dx.doi.org/10.1111/j.1469-8749.1968.tb02954.x.

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22

Martin, Andrés, Kathleen Koenig, Lawrence Scahill, Elaine Tierney, Forbes D. Porter, and Ngozi A. Nwokoro. "SMITH-LEMLI-OPITZ SYNDROME." Journal of the American Academy of Child & Adolescent Psychiatry 40, no. 5 (May 2001): 506–7. http://dx.doi.org/10.1097/00004583-200105000-00008.

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23

Ginat, Sharon, Cheryl L. Maslen, William E. Connor, Forbes D. Porter, and Robert D. Steiner. "Smith-Lemli-Opitz Syndrome." Endocrinologist 10, no. 5 (September 2000): 300–313. http://dx.doi.org/10.1097/00019616-200010050-00004.

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24

Stritzke, Jürgen. "Heinz Opitz 70 Jahre." Bautechnik 84, no. 9 (September 2007): 669–70. http://dx.doi.org/10.1002/bate.200790204.

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25

Israel, Charles W., and M. F. Fierro. "Smith-Lemli-Opitz Syndrome." Developmental Medicine & Child Neurology 19, no. 4 (November 12, 2008): 551. http://dx.doi.org/10.1111/j.1469-8749.1977.tb07956.x.

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26

Meinecke, Peter, Werner Blunck, Alexander Rodewald, John M. Opitz, and James F. Reynolds. "Smith-Lemli-Opitz syndrome." American Journal of Medical Genetics 28, no. 3 (November 1987): 735–39. http://dx.doi.org/10.1002/ajmg.1320280322.

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27

Haas, D., P. Bittigau, C. Hübner, and G. F. Hoffmann. "Smith-Lemli-Opitz-Syndrom." Monatsschrift Kinderheilkunde 145, no. 8 (August 26, 1997): 806–9. http://dx.doi.org/10.1007/s001120050181.

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28

Ludwig, Walther. "DES MARTIN OPITZ EPICEDIUM AUF ERZHERZOG KARL VON 6STERREICH." Daphnis 29, no. 1-2 (March 30, 2000): 177–96. http://dx.doi.org/10.1163/18796583-90000705.

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Als Specimen des von mehreren Mitarbeitem vorbereiteten Opitius Latinus, einer kommentierten Ausgabe der von Martin Opitz verfaßten lateinischen Texte, wird das lateinische Epicedium auf Erzherzog Karl von Österreich (1590-1624) ediert, übersetzt und unter Beachtung seiner Bezüge zur zeigenössischen Trauerdichtung und zur antiken Literatur interpretiert und dabei gezeigt, wie Opitz die konventioneilen Themen Trauer und Trost hier zu einem Panegyricus auf das mit Gott verbundene, weltbeherrschende und ideologisch an die antiken Kaiser anknüpfende Haus Österreich instrumentalisierte.

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29

Harst, Joachim. "MIT GESPALTENER ZUNGE." Daphnis 41, no. 1 (March 30, 2012): 177–202. http://dx.doi.org/10.1163/18796583-90000869.

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Der Beitrag arbeitet markante Modifikationen von Opitz’ Antigone-Übersetzung auf syntaktischer, stilistischer und semantischer Ebene heraus: Während die sophokleische Tragödie vom Oxymoron geprägt ist, zeichnet sich Opitz’ Übersetzung durch die Klärung des paradoxen Ausdrucks zur äußerlichen Antithese aus. Dank ihr kann die Tragödie als moralisches Exempel präsentiert werden. Der Grund für diese Umdichtung wird im rhetorischen Sprachverständnis des Übersetzers gesucht: Die Eigenart seines “Teutschs” (und des von ihm geprägten Trauerspiels) liegt in der zwiespältigen Orientierung an griechischer Tragödie und lateinischer Gerichtsrhetorik begründet.

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30

Opitz, Weston. "Classification, natural history, and evolution of Neorthopleurinae Opitz (Coleoptera, Cleridae). Part III. The Genera Agaphalera Opitz, Allochotes Westwood, Kataspinula Opitz, Lebasiella Spinola, Loedelia Lucas, Patuleius Fairmaire, Rifkindius Opitz, and Romanaeclerus Winkler." Pan-Pacific Entomologist 89, no. 4 (October 2013): 244–58. http://dx.doi.org/10.3956/2013-20.1.

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31

Pelluard-Nehmé, Fanny, Dominique Carles, Eve Marie Alberti, Robert Saura, Christian Wong, and Claude Wolf. "Syndrome de Smith-Lemli-Opitz." Annales de Pathologie 25, no. 4 (September 2005): 318–21. http://dx.doi.org/10.1016/s0242-6498(05)80136-1.

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32

Rivas Crespo, F. "Síndrome de Smith-Lemli-Opitz." Anales de Pediatría 55, no. 1 (2001): 94–95. http://dx.doi.org/10.1016/s1695-4033(01)77637-0.

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33

Kiess, Wieland, Manuela Schulz, Sabine Liebermann, Roland Pfäffle, Peter Bührdel, and Johannes Weigel. "Das Smith-Lemli-Opitz-Syndrom." Kinder- und Jugendmedizin 5, no. 04 (2005): 178–82. http://dx.doi.org/10.1055/s-0037-1617867.

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ZusammenfassungDas Smith-Lemli-Opitz-Syndrom wird durch einen Defekt des letzten Schrittes der Cholesterolbiosynthese, den Mangel an 7-Dehydrocholesterolreduktase, verursacht. Die Akkumulation der Metaboliten 7-Dehydrocholesterol und 8-Dehydrocholesterol, die die wichtigsten biochemischen Marker für die Diagnose der Erkrankung darstellen, sowie der Mangel an Cholesterol können zu multiplen kongenitalen Anomalien führen. Die Ursache des Enzymmangels sind Mutationen innerhalb des DHCR7-Gens, welches auf Chromosom 11q13 lokalisiert ist. Therapeutische Möglichkeiten bestehen in der Gabe von Cholesterol und im Notfall Fresh Frozen Plasma (FFP); der therapeutische Nutzen von Statinen befindet sich zurzeit in der klinischen Erprobung.

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Kelley, R. I. "The Smith-Lemli-Opitz syndrome." Journal of Medical Genetics 37, no. 5 (May 1, 2000): 321–35. http://dx.doi.org/10.1136/jmg.37.5.321.

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MacDonald, Madeleine R., Ann Haskins Olney, and Peg Kolodziej. "Opitz Syndrome (G/BBB Syndrome)." Ear, Nose & Throat Journal 77, no. 7 (July 1998): 528–29. http://dx.doi.org/10.1177/014556139807700706.

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36

Greenhalgh, K. L., R. A. Newbury-Ecob, P. W. Lunt, C. L. Dolling, H. Hargreaves, and S. F. Smithson. "Siblings with Bohring-Opitz syndrome." Clinical Dysmorphology 12, no. 1 (January 2003): 15–20. http://dx.doi.org/10.1097/00019605-200301000-00003.

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De Koster, Jan, Eric Legius, Francis De Zegher, Hugo Devlieger, Jean-Pierre Fryns, and Ephrem Eggermont. "Opitz C syndrome and pseudohypoaldosteronism." American Journal of Medical Genetics 37, no. 4 (December 1990): 457–59. http://dx.doi.org/10.1002/ajmg.1320370405.

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38

Iurian, Sorin Ioan, Livia Ognean, Han Brunner, Leo Kluijtmans, Petr Jira, Dana Fintina, and Bogdan Ionut Mehedintu. "SMITH-LEMLI-OPITZ SYNDROME. CASE REPORT." Romanian Journal of Pediatrics 64, no. 1 (March 31, 2015): 34–37. http://dx.doi.org/10.37897/rjp.2015.1.7.

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Smith-Lemli-Opitz syndrome (SLOS) is an autosomal-recessive inherited disease characterized by multiple anomalies secondary to cholesterol synthesis impairment. The authors present diagnosis peculiarities and limitation of treatment options in a 5-weeks old infant with ambiguous genitalia.

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39

Urreizti, Roser, Neus Roca-Ayats, Judith Trepat, Francisco Garcia-Garcia, Alejandro Aleman, Daniela Orteschi, Giuseppe Marangi, et al. "Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromes." American Journal of Medical Genetics Part A 170, no. 1 (October 7, 2015): 24–31. http://dx.doi.org/10.1002/ajmg.a.37418.

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40

Iurian, Sorin Ioan, Livia Ognean, Han Brunner, Leo Kluijtmans, Petr Jira, Dana Fîntînă, and Bogdan Ionuţ Mehedinţu. "SINDROMUL SMITH-LEMLI-OPITZ. PREZENTARE DE CAZ." Romanian Journal of Pediatrics 64, no. 1 (March 31, 2015): 70–73. http://dx.doi.org/10.37897/rjp.2015.1.15.

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Sindromul Smith-Lemli-Opitz (SSLO) reprezintă o afecţiune cu transmitere autozomal-recesivă caracterizată prin multiple anomalii şi care se datorează anomaliilor în sinteza colesterolului. Autorii prezintă particularităţile diagnostice şi terapeutice la un sugar cu ambiguitate genitală.

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41

Hellwig, Jan. "Geschichte der Mädchen und Frauenbildung. Red. Elke Kleinau, Claudia Opitz. Tom II. Vom Vormärzis zur Gegenwart. Campus Verlag. Frankfurt, New York 1996, ss. 673." Biuletyn Historii Wychowania, no. 9/10 (January 6, 2019): 64–65. http://dx.doi.org/10.14746/bhw.1999.9.10.20.

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42

Opitz, Weston. "Classification, Natural History, and Evolution of the Orthopleurinae (Coleoptera: Cleridae). Part VI. The New Genera Coadnatus Opitz, Furcadia Opitz, and Latupusillus Opitz, One New Species of Funicula Opitz, and Four New Species of Romanaeclerus Winkler." Coleopterists Bulletin 71, no. 3 (September 18, 2017): 421. http://dx.doi.org/10.1649/0010-065x-71.3.421.

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43

Castilla-Vallmanya, Urreizti, Franco, Amiel, Tan, Neumann, Gordon, and Grinberg. "Understanding the Pathophysiology and Searching for Biomarkers for Rare Genetic Developmental Diseases." Proceedings 22, no. 1 (August 8, 2019): 53. http://dx.doi.org/10.3390/proceedings2019022053.

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Opitz C syndrome (OCS, MIM #211750) is an extremely rare genetic disorder characterized bymultiple malformations (e.g., trigonocephaly, congenital heart defects) and variable intellectual andpsychomotor delay. [...]

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Antunes-Foschini, Rosália M. S., and Harley E. A. Bicas. "Síndrome de Opitz: relato de caso." Arquivos Brasileiros de Oftalmologia 63, no. 2 (April 2000): 151–54. http://dx.doi.org/10.1590/s0004-27492000000200012.

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Terrisse, Bénédicte. "Michael Opitz, Wolfgang Hilbig. Eine Biographie." Germanica, no. 61 (December 31, 2017): 133–41. http://dx.doi.org/10.4000/germanica.4131.

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Haghiri, N., A. Menget, V. Laitier, C. Fromentin, F. Nocton, and N. Kalach. "Le syndrome de Smith-Lemli-Opitz." Archives de Pédiatrie 6, no. 5 (May 1999): 536–39. http://dx.doi.org/10.1016/s0929-693x(99)80561-2.

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Kazartsev, Evgeny. "Niederländische Quellen von Martin Opitz' Versrhythmik." Zeitschrift für Germanistik 23, no. 3 (January 1, 2013): 499–509. http://dx.doi.org/10.3726/92140_499.

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Kelly, Maria N., Sanjeev Y. Tuli, Sonal S. Tuli, Mori A. Stern, and Beverly P. Giordano. "Brothers With Smith-Lemli-Opitz Syndrome." Journal of Pediatric Health Care 29, no. 1 (January 2015): 97–103. http://dx.doi.org/10.1016/j.pedhc.2014.04.006.

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Sargent, C., J. Burn, M. Baraitser, and M. E. Pembrey. "Trigonocephaly and the Opitz C syndrome." Journal of Medical Genetics 22, no. 1 (February 1, 1985): 39–45. http://dx.doi.org/10.1136/jmg.22.1.39.

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Schoolfield, George. "Propertius and Opitz: A Compound Footnote." Daphnis 21, no. 1 (January 3, 1992): 27–43. http://dx.doi.org/10.1163/18796583-02101004.

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