Artículos de revistas sobre el tema "Genetic disorders in children"
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Ćirić, Sanela. "DIFFERENCES IN PARENTS' ATTITUDES TOWARDS THE CAUSES OF NEURODEVELOPMENTAL DISORDERS". Multidisciplinarni Pristupi u Edukaciji i Rehabilitaciji 6, n.º 7 (15 de agosto de 2024): 161–70. http://dx.doi.org/10.59519/mper6115.
Texto completoFisch, Gene S., Nancy Carpenter, Patricia N. Howard-Peebles, Jeanette J. A. Holden, Jack Tarleton, Richard Simensen y Agatino Battaglia. "Developmental Trajectories in Syndromes With Intellectual Disability, With a Focus on Wolf-Hirschhorn and Its Cognitive–Behavioral Profile". American Journal on Intellectual and Developmental Disabilities 117, n.º 2 (1 de febrero de 2012): 167–79. http://dx.doi.org/10.1352/1944-7558-117.2.167.
Texto completoLashwood, Alison. "Preimplantation genetic diagnosis to prevent genetic disorders in children". British Journal of Nursing 14, n.º 2 (enero de 2005): 64–70. http://dx.doi.org/10.12968/bjon.2005.14.2.17433.
Texto completoBarrie, Alpha-Umaru. "Youth perspectives on genetic inheritance, carrier status and disclosure". Journal of Haemophilia Practice 3, n.º 2 (1 de julio de 2016): 21–28. http://dx.doi.org/10.17225/jhp00077.
Texto completoRudin, I. V. "SPEECH DISORDERS OF GENETIC ORIGIN IN TEACHING PRACTICE". Education & Pedagogy Journal, n.º 1(1) (6 de julio de 2021): 56–63. http://dx.doi.org/10.23951/2782-2575-2021-1-56-63.
Texto completoMueller, Sven C., Pamela Ng, Ninet Sinaii, Ellen W. Leschek, Liza Green-Golan, Carol VanRyzin, Monique Ernst y Deborah P. Merke. "Psychiatric characterization of children with genetic causes of hyperandrogenism". European Journal of Endocrinology 163, n.º 5 (noviembre de 2010): 801–10. http://dx.doi.org/10.1530/eje-10-0693.
Texto completoZhestkova, M. A. y D. Yu Ovsyannikov. "GENETIC DISORDERS OF SURFACTANT PROTEINS". Pediatria. Journal named after G.N. Speransky 100, n.º 5 (11 de octubre de 2021): 82–89. http://dx.doi.org/10.24110/0031-403x-2021-100-5-82-89.
Texto completoYou, Haizhen, Junyao Shi, Fangfang Huang, Zhiyun Wei, Gary Jones, Wenchong Du y Jing Hua. "Advances in Genetics and Epigenetics of Developmental Coordination Disorder in Children". Brain Sciences 13, n.º 6 (11 de junio de 2023): 940. http://dx.doi.org/10.3390/brainsci13060940.
Texto completoPletcher, Beth A. y Nelson L. Turcios. "Pulmonary Manifestations of Genetic Disorders in Children". Pediatric Clinics of North America 68, n.º 1 (febrero de 2021): 1–24. http://dx.doi.org/10.1016/j.pcl.2020.09.010.
Texto completoClauss, Sarah B. y Peter O. Kwiterovich. "Genetic disorders of lipoprotein transport in children". Progress in Pediatric Cardiology 17, n.º 2 (septiembre de 2003): 123–33. http://dx.doi.org/10.1016/s1058-9813(03)00049-3.
Texto completoMorozova, E. A., M. V. Belousova, D. V. Morozov, D. I. Gabelko y V. V. Bogolyubova. "Genetic aspects of speech disorders in children". Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova 123, n.º 9 (2023): 87. http://dx.doi.org/10.17116/jnevro202312309287.
Texto completoFrans, E. M., P. Lichtenstein, C. M. Hultman y R. Kuja-Halkola. "Age at fatherhood: heritability and associations with psychiatric disorders". Psychological Medicine 46, n.º 14 (12 de agosto de 2016): 2981–88. http://dx.doi.org/10.1017/s0033291716001744.
Texto completoFelsenfeld, Susan y Robert Plomin. "Epidemiological and Offspring Analyses of Developmental Speech Disorders Using Data From the Colorado Adoption Project". Journal of Speech, Language, and Hearing Research 40, n.º 4 (agosto de 1997): 778–91. http://dx.doi.org/10.1044/jslhr.4004.778.
Texto completoPak, Lale A., Kirill V. Savostyanov, Lyudmila M. Kuzenkova, Alexander A. Pushkov, Ilya S. Zhanin y Eugeniya V. Uvakina. "Molecular genetic diagnosis of speech disorders in children". L.O. Badalyan Neurological Journal 3, n.º 1 (30 de marzo de 2022): 7–13. http://dx.doi.org/10.46563/2686-8997-2022-3-1-7-13.
Texto completoLuhrs, Kyleen, Tracey Ward, Caitlin M. Hudac, Jennifer Gerdts, Holly A. F. Stessman, Evan E. Eichler y Raphael A. Bernier. "Associations between Familial Rates of Psychiatric Disorders and De Novo Genetic Mutations in Autism". Autism Research and Treatment 2017 (2017): 1–9. http://dx.doi.org/10.1155/2017/9371964.
Texto completoCerniglia, Luca. "Neurobiological, Genetic, and Epigenetic Foundations of Eating Disorders in Youth". Children 11, n.º 3 (23 de febrero de 2024): 274. http://dx.doi.org/10.3390/children11030274.
Texto completoGlotov, O. S., A. N. Chernov, P. A. Suchko, Yu A. Eismont y L. A. Mayorova. "Formation of cognitive processes in children with autism. Part II. Genetic mechanisms". Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 69, n.º 2 (8 de mayo de 2024): 26–33. http://dx.doi.org/10.21508/1027-4065-2024-69-2-26-33.
Texto completoKuraeva, Tamara Leonidovna, Elena Aleksandrovna Sechko, Lubov' Iosifovna Zilberman, Olga Nikolaevna Ivanova, Aleksandr Yurievich Mayorov, Ekaterina Olegovna Koksharova, Valentina Aleksandrovna Peterkova y Ivan Ivanovich Dedov. "Molecular genetic and clinical variants MODY2 and MODY3 in children in Russia". Problems of Endocrinology 61, n.º 5 (28 de enero de 2016): 14–25. http://dx.doi.org/10.14341/probl201561514-25.
Texto completoBelousova, E. D., O. S. Groznova y V. Yu Voinova. "Genome-wide sequencing in children with epilepsy and developmental disorders". Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 69, n.º 2 (10 de mayo de 2024): 56–64. http://dx.doi.org/10.21508/1027-4065-2024-69-2-56-64.
Texto completoCop, Esra, Pinar Yurtbasi, Ozgur Oner y Kerim Munir. "Genetic testing in children with autism spectrum disorders". Anatolian Journal of Psychiatry 16, n.º 6 (2015): 426. http://dx.doi.org/10.5455/apd.1414607917.
Texto completoMokhtar, M. M. "Chromosomal aberrations in children with suspected genetic disorders". Eastern Mediterranean Health Journal 3, n.º 1 (15 de enero de 1997): 114–22. http://dx.doi.org/10.26719/1997.3.1.114.
Texto completoClarke, David. "Handbook of Neurodevelopmental and Genetic Disorders in Children". Journal of Applied Research in Intellectual Disabilities 14, n.º 4 (diciembre de 2001): 420–21. http://dx.doi.org/10.1111/j.1468-3148.2001.00080.x.
Texto completoGoldson, Edward. "Handbook of Neurodevelopmental and Genetic Disorders in Children",. Journal of Developmental & Behavioral Pediatrics 21, n.º 4 (agosto de 2000): 307–8. http://dx.doi.org/10.1097/00004703-200008000-00013.
Texto completoTully, Elizabeth M. "Handbook of Neurodevelopmental and Genetic Disorders in Children". Journal of the American Academy of Child & Adolescent Psychiatry 39, n.º 7 (julio de 2000): 935. http://dx.doi.org/10.1097/00004583-200007000-00026.
Texto completoDONNELLY, CRAIG L. "Handbook of Neurodevelopmental and Genetic Disorders in Children". American Journal of Psychiatry 159, n.º 6 (junio de 2002): 1070–71. http://dx.doi.org/10.1176/appi.ajp.159.6.1070.
Texto completoRapin, Isabelle. "Handbook of neurodevelopmental and genetic disorders in children". Annals of Neurology 47, n.º 3 (marzo de 2000): 415. http://dx.doi.org/10.1002/1531-8249(200003)47:3<415::aid-ana29>3.0.co;2-b.
Texto completoMaritska, Ziske, Atikah M. Ihsan, Ina Rahmawati, Perawati Perawati, Mohammad Hilal Atthariq Ramadhan, Bintang Arroyantri Prananjaya y Nita Parisa. "Genetic Conditions Associated with Intellectual Disability in Indonesian Population: A Review". Sriwijaya Journal of Medicine 7, n.º 1 (10 de junio de 2024): 8–15. http://dx.doi.org/10.32539/sjm.v7i1.220.
Texto completoChen, Lei-Shih, Jungkyung Min, Shixi Zhao, Yu-Chen Yeh y Tse-Yang Huang. "Information needs in genetic testing: A needs assessment survey among Taiwanese parents of children with autism spectrum disorders". Autism 23, n.º 4 (3 de agosto de 2018): 902–9. http://dx.doi.org/10.1177/1362361318778903.
Texto completoGavryutina, Irina, Lawrence Fordjour y Vivian L. Chin. "Genetics of Thyroid Disorders". Endocrines 3, n.º 2 (13 de abril de 2022): 198–213. http://dx.doi.org/10.3390/endocrines3020018.
Texto completoWaters, A. M., B. P. Bradley y K. Mogg. "Biased attention to threat in paediatric anxiety disorders (generalized anxiety disorder, social phobia, specific phobia, separation anxiety disorder) as a function of ‘distress’versus‘fear’ diagnostic categorization". Psychological Medicine 44, n.º 3 (17 de abril de 2013): 607–16. http://dx.doi.org/10.1017/s0033291713000779.
Texto completoGorchkhanova, Z. K., E. A. Nikolaeva, S. V. Bochenkov y E. D. Belousova. "Clinical manifestations of Angelman syndrome in children". Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 66, n.º 6 (19 de enero de 2022): 63–70. http://dx.doi.org/10.21508/1027-4065-2021-66-6-63-70.
Texto completoLelii, Mara, Elena Baggi, Laura Senatore, Maria Francesca Bedeschi, Robertino Dilena, Maria Iascone, Silvana Gangi, Paola Marchisio y Maria Francesca Patria. "Familial Sleep Disorders in Unknown Genetic Syndrome". Journal of Pediatric Genetics 09, n.º 02 (21 de octubre de 2019): 132–36. http://dx.doi.org/10.1055/s-0039-1698808.
Texto completoLense, Miriam D., Eniko Ladányi, Tal-Chen Rabinowitch, Laurel Trainor y Reyna Gordon. "Rhythm and timing as vulnerabilities in neurodevelopmental disorders". Philosophical Transactions of the Royal Society B: Biological Sciences 376, n.º 1835 (23 de agosto de 2021): 20200327. http://dx.doi.org/10.1098/rstb.2020.0327.
Texto completoGuzeva, Valentina I., Yulia A. Eremkina, Oksana V. Guzeva, Viktoriya V. Guzeva, Damir A. Malekov y Viktoriya A. Vedernikova. "Speech disorders in genetically determined forms of epilepsy in children. Clinical observations". Russian Military Medical Academy Reports 42, n.º 4 (9 de diciembre de 2023): 437–44. http://dx.doi.org/10.17816/rmmar585236.
Texto completoSorasio, Lorena, Luisa Franceschi, Lisa Pavinato y Antonella Peduto. "Quando il disturbo del neurosviluppo ha un substrato genetico: un caso di sindrome di Kleefstra". Medico e Bambino pagine elettroniche 24, n.º 4 (30 de abril de 2021): 114–17. http://dx.doi.org/10.53126/mebxxiv114.
Texto completoBOLTON, DEREK, THALIA C. ELEY, THOMAS G. O'CONNOR, SEAN PERRIN, SOPHIA RABE-HESKETH, FRÜHLING RIJSDIJK y PATRICK SMITH. "Prevalence and genetic and environmental influences on anxiety disorders in 6-year-old twins". Psychological Medicine 36, n.º 3 (17 de noviembre de 2005): 335–44. http://dx.doi.org/10.1017/s0033291705006537.
Texto completoBiesecker, Leslie G. "Clinical Commentary: The Law of Unintended Ethics". Journal of Law, Medicine & Ethics 25, n.º 1 (1997): 16–18. http://dx.doi.org/10.1111/j.1748-720x.1997.tb01390.x.
Texto completoBanu, Meraj, Akbar Ali Khan Pathan y K. V. Chaitanya. "Diagnostics for Genetically Inherited Disorders: From Cytogenetics to Genomics Technologies- A Review". Biomedical and Pharmacology Journal 16, n.º 2 (30 de junio de 2023): 639–51. http://dx.doi.org/10.13005/bpj/2646.
Texto completoFolstein, Susan E. y Joseph Piven. "Etiology of Autism: Genetic Influences". Pediatrics 87, n.º 5 (1 de mayo de 1991): 767–73. http://dx.doi.org/10.1542/peds.87.5.767.
Texto completoVolgina, S. Ya, A. R. Ahmetova, L. K. Shaidukova, N. V. Zhurkova y G. A. Kulakova. "The role of risk factors in the development of speech and language disorders in preschool children". Kazan medical journal 102, n.º 4 (8 de agosto de 2021): 537–44. http://dx.doi.org/10.17816/kmj2021-537.
Texto completoErbeli, Florina, Marianne Rice y Silvia Paracchini. "Insights into Dyslexia Genetics Research from the Last Two Decades". Brain Sciences 12, n.º 1 (26 de diciembre de 2021): 27. http://dx.doi.org/10.3390/brainsci12010027.
Texto completoKalibataitė, Irma, Vilius Rutkauskas, Eglė Preikšaitienė y Vaidutis Kučinskas. "Establishing genetic diagnosis of intellectual disability in children: diagnostic yield of various genetic approaches". Acta medica Lituanica 19, n.º 4 (31 de enero de 2013): 409–15. http://dx.doi.org/10.6001/actamedica.v19i4.2550.
Texto completoGlotov, O. S., A. N. Chernov, P. A. Suchko, Yu A. Eismont y L. A. Mayorova. "Formation of cognitive processes in children with autism. Part I. Epigenetic mechanisms". Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 69, n.º 1 (7 de marzo de 2024): 34–44. http://dx.doi.org/10.21508/1027-4065-2024-69-1-34-44.
Texto completoSnetkov, A. I. "Diagnosis of genetic forms of rickets in children". N.N. Priorov Journal of Traumatology and Orthopedics 1, n.º 3 (15 de septiembre de 1994): 30–33. http://dx.doi.org/10.17816/vto105072.
Texto completoMountford, Hayley S. y Dianne F. Newbury. "The genomic landscape of language: Insights into evolution". Journal of Language Evolution 3, n.º 1 (8 de diciembre de 2017): 49–58. http://dx.doi.org/10.1093/jole/lzx019.
Texto completoNeumann, Alexander, Ilja M. Nolte, Irene Pappa, Tarunveer S. Ahluwalia, Erik Pettersson, Alina Rodriguez, Andrew Whitehouse et al. "A genome-wide association study of total child psychiatric problems scores". PLOS ONE 17, n.º 8 (22 de agosto de 2022): e0273116. http://dx.doi.org/10.1371/journal.pone.0273116.
Texto completoRogers, Maureen. "Nail manifestations of some important genetic disorders in children". Dermatologic Therapy 15, n.º 2 (junio de 2002): 111–20. http://dx.doi.org/10.1046/j.1529-8019.2002.01515.x.
Texto completoKarmiloff-Smith, A., D. D'Souza, T. M. Dekker, J. Van Herwegen, F. Xu, M. Rodic y D. Ansari. "Genetic and environmental vulnerabilities in children with neurodevelopmental disorders". Proceedings of the National Academy of Sciences 109, Supplement_2 (8 de octubre de 2012): 17261–65. http://dx.doi.org/10.1073/pnas.1121087109.
Texto completoAndersson, Nadine G., Maria Rossing, Marcus Fager Ferrari, Migle Gabrielaite, Eva Leinøe, Rolf Ljung, Annika Mårtensson, Eva Norström y Eva Zetterberg. "Genetic screening of children with suspected inherited bleeding disorders". Haemophilia 26, n.º 2 (marzo de 2020): 314–24. http://dx.doi.org/10.1111/hae.13948.
Texto completoHildebrand, Michael S., Victoria E. Jackson, Thomas S. Scerri, Olivia Van Reyk, Matthew Coleman, Ruth O. Braden, Samantha Turner et al. "Severe childhood speech disorder". Neurology 94, n.º 20 (28 de abril de 2020): e2148-e2167. http://dx.doi.org/10.1212/wnl.0000000000009441.
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