Literatura académica sobre el tema "Genetic disorders"
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Artículos de revistas sobre el tema "Genetic disorders"
RUTTER, MICHAEL. "Pathways of genetic influences on psychopathology". European Review 12, n.º 1 (febrero de 2004): 19–33. http://dx.doi.org/10.1017/s1062798704000031.
Texto completoSouery, D., I. Massat y J. Mendlewicz. "Genetics of bipolar disorders". Acta Neuropsychiatrica 12, n.º 3 (septiembre de 2000): 65–68. http://dx.doi.org/10.1017/s0924270800035420.
Texto completoPinheiro, Andréa Poyastro, Patrick F. Sullivan, Josue Bacaltchuck, Pedro Antonio Schmidt do Prado-Lima y Cynthia M. Bulik. "Genetics in eating disorders: extending the boundaries of research". Revista Brasileira de Psiquiatria 28, n.º 3 (9 de agosto de 2006): 218–25. http://dx.doi.org/10.1590/s1516-44462006005000004.
Texto completoMokhtar, M. M., S. M. Kotb y S. R. Ismail. "Autosomal recessive disorders among patients attending the genetics clinic in Alexandria". Eastern Mediterranean Health Journal 4, n.º 3 (15 de mayo de 1998): 470–79. http://dx.doi.org/10.26719/1998.4.3.470.
Texto completoDomschke, K. "Genetics in anxiety disorders - an update". European Psychiatry 26, S2 (marzo de 2011): 2097. http://dx.doi.org/10.1016/s0924-9338(11)73800-7.
Texto completoSouery, D. y J. Mendlewicz. "Molecular genetic findings in mood disorders". Acta Neuropsychiatrica 11, n.º 2 (junio de 1999): 67–70. http://dx.doi.org/10.1017/s092427080003619x.
Texto completoKeller, Matthew C. y Geoffrey Miller. "Resolving the paradox of common, harmful, heritable mental disorders: Which evolutionary genetic models work best?" Behavioral and Brain Sciences 29, n.º 4 (agosto de 2006): 385–404. http://dx.doi.org/10.1017/s0140525x06009095.
Texto completoSouery, D. y J. Mendlewicz. "New molecular genetic findings in the genetics of affective disorders". Acta Neuropsychiatrica 9, n.º 2 (junio de 1997): 52–54. http://dx.doi.org/10.1017/s0924270800036784.
Texto completoBishop, Kathleen Kirk. "Psychosocial Aspects of Genetic Disorders: Implications for Practice". Families in Society: The Journal of Contemporary Social Services 74, n.º 4 (abril de 1993): 207–12. http://dx.doi.org/10.1177/104438949307400402.
Texto completoLeonard, J. V. "Genetic Biochemical Disorders". Journal of Medical Genetics 23, n.º 4 (1 de agosto de 1986): 378. http://dx.doi.org/10.1136/jmg.23.4.378.
Texto completoTesis sobre el tema "Genetic disorders"
Melin, Malin. "Identification of Candidate Genes in Four Human Disorders". Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-7344.
Texto completoFung, Hon Chung. "Genetic characterisation of neurodegenerative disorders". Thesis, University College London (University of London), 2007. http://discovery.ucl.ac.uk/4930/.
Texto completoSchneider, Katja Susanne Annika. "Electrophysiological biomarkers in genetic movement disorders". Thesis, University College London (University of London), 2008. http://discovery.ucl.ac.uk/15926/.
Texto completoMigdalska, Anna Marta. "Modelling human genetic disorders in mice". Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610341.
Texto completoLeiser, Kimberly A. "Assessing the association between the increased resolution of the signaturechip WG and the abnormality detection rate". Pullman, Wash. : Washington State University, 2009. http://www.dissertations.wsu.edu/Thesis/Spring2009/k_leiser_042709.pdf.
Texto completoTitle from PDF title page (viewed on June 5, 2009). "Department of Health Policy and Administration." Includes bibliographical references (p. 34-39).
Spataro, Nino 1984. "Human genetic disorders: Mendelian and complex diseases". Doctoral thesis, Universitat Pompeu Fabra, 2016. http://hdl.handle.net/10803/482220.
Texto completoDes de l'Origen de les Espècies de Darwin van passar molts anys abans que les malalties humanes fossin considerades sota un marc evolutiu. Tanmateix, tot i els darrers avenços teòrics i empírics, estem molt lluny de tenir una comprensió completa de l'etiologia de les malalties humanes. Mentre els trastorns altament penetrants amb herència mendeliana poden explicar-se sota un model d’equilibri mutació-selecció, aquest és insuficient per descriure les pressions selectives que actuen sobre tot el conjunt d'al·lels associats a malalties. Mostrem en els dos primers treballs que les noves tecnologies de seqüenciació proporcionen una oportunitat única per investigar la variació i contribuir a la comprensió de l'arquitectura genètica de la malaltia. A més d'explorar el paper de les variants rares i en el nombre de còpies en la malaltia de Parkinson (PD), demostrem la relació funcional entre les formes mendelianes i idiopàtiques d’aquesta malaltia. En el darrer treball, mostrem sota una perspectiva evolutiva i funcional que, en comparació amb la variació genètica en gens associats només a malalties complexes, la variació en gens prèviament relacionats amb trastorns Mendelians sembla tenir un paper clarament més important en la susceptibilitat a la malaltia complexa.
Valente, Enza Maria. "Movement disorders : a clinical and genetic study". Thesis, University College London (University of London), 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.405854.
Texto completoDubois, Patrick Charles Alexander. "Genetic risk variants in intestinal inflammatory disorders". Thesis, Queen Mary, University of London, 2010. http://qmro.qmul.ac.uk/xmlui/handle/123456789/704.
Texto completoLiskova, P. "Molecular genetic study of inherited corneal disorders". Thesis, University College London (University of London), 2009. http://discovery.ucl.ac.uk/18007/.
Texto completoChen, Huijia. "Skin barrier dysfunction in common genetic disorders". Thesis, University of Dundee, 2011. https://discovery.dundee.ac.uk/en/studentTheses/37ccdf72-e6b2-43e2-b5a0-954be5cb6811.
Texto completoLibros sobre el tema "Genetic disorders"
Parks, Peggy J. Genetic disorders. San Diego, CA: ReferencePoint Press, 2009.
Buscar texto completoKatherine, Swarts, ed. Genetic disorders. Detroit: Greenhaven Press, 2009.
Buscar texto completoParks, Peggy J. Genetic disorders. San Diego, CA: ReferencePoint Press, 2009.
Buscar texto completoParks, Peggy J. Genetic disorders. San Diego, CA: ReferencePoint Press, 2009.
Buscar texto completoAngelini, Corrado. Genetic Neuromuscular Disorders. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-56454-8.
Texto completoAngelini, Corrado. Genetic Neuromuscular Disorders. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-07500-6.
Texto completoBenson, P. F. Genetic biochemical disorders. Oxford: Oxford University Press, 1986.
Buscar texto completoBenson, P. F. Genetic biochemical disorders. Oxford: Oxford University Press, 1985.
Buscar texto completoBenson, P. F. Genetic biochemical disorders. Oxford [Oxfordshire]: Oxford University Press, 1985.
Buscar texto completoSybert, Virginia P. Genetic skin disorders. 2a ed. New York: Oxford University Press, 2010.
Buscar texto completoCapítulos de libros sobre el tema "Genetic disorders"
Massart, Mylynda Beryl. "Genetic Disorders". En Family Medicine, 205–16. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-04414-9_16.
Texto completoBachman, John W. "Genetic Disorders". En Family Medicine, 138–45. New York, NY: Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4757-2947-4_16.
Texto completoBachman, John W. "Genetic Disorders". En Family Medicine, 141–48. New York, NY: Springer New York, 2003. http://dx.doi.org/10.1007/978-0-387-21744-4_16.
Texto completoMassart, Mylynda Beryl. "Genetic Disorders". En Family Medicine, 1–12. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-1-4939-0779-3_16-1.
Texto completoMassart, Mylynda Beryl. "Genetic Disorders". En Family Medicine, 1–15. New York, NY: Springer New York, 2020. http://dx.doi.org/10.1007/978-1-4939-0779-3_16-2.
Texto completoAwaad, Yasser M. "Genetic Disorders". En Absolute Pediatric Neurology, 29–116. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-78801-2_3.
Texto completoScahill, Lawrence David, Koorosh Kooros, Ramon Barinaga, Rechele Brooks, Marisela Huerta, Lindsey Sterling, Jeffrey J. Wood et al. "Genetic Disorders". En Encyclopedia of Autism Spectrum Disorders, 1432. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-1698-3_100640.
Texto completoChaitanya, K. V. "Genetic Disorders". En Diagnostics and Gene Therapy for Human Genetic Disorders, 81–115. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003343790-3.
Texto completoLaskaris, George y Crispian Scully. "Genetic Disorders". En Periodontal Manifestations of Local and Systemic Diseases, 119–57. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-642-55596-1_16.
Texto completoBaum, Andrew S. y John P. Garofalo. "Genetic disorders." En Encyclopedia of Psychology, Vol. 3., 464–66. Washington: American Psychological Association, 2000. http://dx.doi.org/10.1037/10518-221.
Texto completoActas de conferencias sobre el tema "Genetic disorders"
Lugo-Ramos, L. E., M. Collazo-Roman, D. De Sola y W. De Jesus-Rojas. "Case Series: Pediatric Sleep-Disordered Breathing in Rare Genetic Disorders". En American Thoracic Society 2021 International Conference, May 14-19, 2021 - San Diego, CA. American Thoracic Society, 2021. http://dx.doi.org/10.1164/ajrccm-conference.2021.203.1_meetingabstracts.a3481.
Texto completoRogers, Ian y Ranjan Srivastava. "Using ensemble modeling to determine causes of multifactorial disorders". En GECCO '18: Genetic and Evolutionary Computation Conference. New York, NY, USA: ACM, 2018. http://dx.doi.org/10.1145/3205651.3205686.
Texto completoRülke, Franziska, Susan Arndt, Antje Aschendorff, Andreas Knopf y Ralf Birkenhäger. "Systematic characterization of non-syndromal genetic hearing disorders". En Abstract- und Posterband – 91. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn – Welche Qualität macht den Unterschied. © Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1711205.
Texto completoHanenberg, H. "Delivery systems for genetic therapies of hematological disorders". En HÄMATOLOGIE HEUTE 2019. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1684056.
Texto completoBEZZINA, CONNIE R. y ARTHUR A. M. WILDE. "MOLECULAR, GENETIC AND CLINICAL ASPECTS OF ARRHYTHMIA DISORDERS". En Proceedings of the 31st International Congress on Electrocardiology. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812702234_0080.
Texto completoKabeya, Yoshinori, Toshiya Iwamori, Sho Yonezawa, Yusuke Takeuchi, Hiroki Nakano, Yuhe Nagisa, Mariko Okubo et al. "Physician-Level Aggregated Classifier for Genetic Muscle Disorders". En 2019 IEEE 16th International Symposium on Biomedical Imaging (ISBI). IEEE, 2019. http://dx.doi.org/10.1109/isbi.2019.8759409.
Texto completoAli, Rehab. "Duchenne Muscular Dystrophy, Clinical and Genetic Spectrum in Qatar". En Congenital Dystrophies - Neuromuscular Disorders Precision Medicine: Genomics to Care and Cure. Hamad bin Khalifa University Press (HBKU Press), 2020. http://dx.doi.org/10.5339/qproc.2020.nmd.15.
Texto completoNayır Büyükşahin, H., N. Emiralioglu, P. O. Simsek Kiper, B. Sunman, I. Güzelkaş, D. Alboğa, M. Akgül Erdal et al. "Evaluation of polysomnography findings in children with genetic skeletal disorders". En ERS International Congress 2022 abstracts. European Respiratory Society, 2022. http://dx.doi.org/10.1183/13993003.congress-2022.526.
Texto completoSmid, Jerusa, Ricardo Nitrini, Vilma Martins, Michele Landemberger, Helio Gomes, Nathalie Canedo Canedo y Leila Chimelli. "THE BRAZILIAN SURVEILLANCE FOR PRION DISEASE: CURRENT DATA". En XIII Meeting of Researchers on Alzheimer's Disease and Related Disorders. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1980-5764.rpda014.
Texto completoFando, Roman y Maria Klavdieva. "Biotechnology and Computer Modeling on the Way to Treating Genetic Disorders". En 2017 International Workshop on Engineering Technologies and Computer Science (EnT). IEEE, 2017. http://dx.doi.org/10.1109/ent.2017.13.
Texto completoInformes sobre el tema "Genetic disorders"
Andrews, Lori, B. Complex Genetic Disorders and Intellectual Property Rights Final Report. Office of Scientific and Technical Information (OSTI), noviembre de 2006. http://dx.doi.org/10.2172/895052.
Texto completoAndrews, Lori. Ethical and legal issues arising from complex genetic disorders. DOE final report. Office of Scientific and Technical Information (OSTI), octubre de 2002. http://dx.doi.org/10.2172/805433.
Texto completoZhenni, Mu, Le Lei, Shen Sinan y Tang Li. Effectiveness of integrated Chinese herbal medicine Shoutai Pill and Western medicine in the treatment of recurrent pregnancy loss: A protocol for systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, octubre de 2021. http://dx.doi.org/10.37766/inplasy2021.10.0062.
Texto completoFigueredo, Luisa, Liliana Martinez y Joao Paulo Almeida. Current role of Endoscopic Endonasal Approach for Craniopharyngiomas. A 10-year Systematic review and Meta-Analysis Comparison with the Open Transcranial Approach. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, enero de 2023. http://dx.doi.org/10.37766/inplasy2023.1.0045.
Texto completoPaul, Satashree. Autism Spectrum Disorder. Science Repository, febrero de 2021. http://dx.doi.org/10.31487/sr.blog.26.
Texto completoBhaskar Kalarani, Iyshwarya y Ramakrishnan Veerabathiran. Study of genetic polymorphisms in autism spectrum disorder. Peeref, octubre de 2022. http://dx.doi.org/10.54985/peeref.2210p6305148.
Texto completoZhian, Samaneh. Molecular Genetic Analysis of CRELD1 in Patients with Heterotaxy Disorder. Portland State University Library, enero de 2000. http://dx.doi.org/10.15760/etd.410.
Texto completoGupta, Shweta. The Disorder That Makes One Age 7 Times Faster. Science Repository OÜ, noviembre de 2020. http://dx.doi.org/10.31487/sr.blog.13.
Texto completoTaub, Daniel y Joshua Page. Cystic Fibrosis: Exploration of Evolutionary Explanations for the High Frequency of a Common Genetic Disorder. Genetics Society of America Peer-Reviewed Education Portal (GSA PREP), octubre de 2013. http://dx.doi.org/10.1534/gsaprep.2013.004.
Texto completoUnderstanding eating disorder susceptibility requires an integrated sociological, biological and genetic approach. ACAMH, julio de 2018. http://dx.doi.org/10.13056/acamh.10564.
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