Medical genetics is the branch of medicine that involves the diagnosis and management of hereditary disorders. Medical genetics differs from human genetics...
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The medical genetics of Jews have been studied to identify and prevent some rare genetic diseases that, while still rare, are more common than average...
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Journal of Medical Genetics Part A American Journal of Medical Genetics Part B: Neuropsychiatric Genetics American Journal of Medical Genetics Part C: Seminars...
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Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 175 (1): 8–26. doi:10.1002/ajmg.c.31552. PMID 28306229. S2CID 4440499. "Genetics and Inheritance...
108 KB (11,172 words) - 13:36, 1 October 2024
Genetics is the study of genes, genetic variation, and heredity in organisms. It is an important branch in biology because heredity is vital to organisms'...
98 KB (10,409 words) - 04:06, 29 September 2024
the genetics of human life. This article describes only basic features of human genetics; for the genetics of disorders please see: medical genetics. For...
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Brachydactyly type D (section Genetics)
anomalies of the hands and feet: A new genetic trait". American Journal of Medical Genetics. 10 (3): 245–55. doi:10.1002/ajmg.1320100308. ISSN 1096-8628. PMID 6272576...
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make-up syndrome: a review". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 117C (1): 57–65. doi:10.1002/ajmg.c.10020. PMID 12561059...
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The Journal of Medical Genetics is a monthly peer-reviewed medical journal covering all aspects of medical genetics, including reviews of and opinion on...
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health rather than individual health). Medical genetics – the application of genetics to medicine. Medical genetics is a broad and varied field. It encompasses...
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contractures, and severe cardiac valve insufficiency". Journal of Medical Genetics. 28 (4): 267–273. doi:10.1136/jmg.28.4.267. ISSN 0022-2593. PMC 1016831...
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Jacobsen syndrome (section Genetics)
been reported of Jacobsen syndrome in medical literature. Reference, Genetics Home. "Jacobsensyndrome". Genetics Home Reference. "Jacobsen Syndrome". prezi...
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anomalies in a large cohort of boys with 49, XXXXY". American Journal of Medical Genetics. 163 (1): 44–49. doi:10.1002/ajmg.c.31354. PMID 23359596. S2CID 40989726...
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XX male syndrome (section Genetics)
chromosome abnormalities". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 184 (2): 202–215. doi:10.1002/ajmg.c.31805. PMID 32506765...
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PhD in genetics and undertakes research and/or lectures in the field. A medical geneticist is a physician who has been trained in medical genetics as a...
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girls with a rare chromosomal disorder, 48,XXXX". American Journal of Medical Genetics Part A. 167A (10): 2251–2259. doi:10.1002/ajmg.a.37198. PMID 26086740...
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Bohring–Opitz syndrome (section Genetics)
Bohring–Opitz syndrome caused by de novo ASXL1 mutations". American Journal of Medical Genetics Part A. 158A (4): 917–921. doi:10.1002/ajmg.a.35265. PMID 22419483...
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Marfan syndrome (section Genetics)
"The revised Ghent nosology for the Marfan syndrome". Journal of Medical Genetics. 47 (7): 476–485. doi:10.1136/jmg.2009.072785. hdl:1854/LU-1013955...
73 KB (6,848 words) - 16:42, 16 September 2024
Treacher Collins syndrome (section Genetics)
using combined linkage analysis and ultrasound imaging". Journal of Medical Genetics. 33 (7): 603–606. doi:10.1136/jmg.33.7.603. PMC 1050672. PMID 8818950...
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case with pentasomy X and novel clinical findings". Balkan Journal of Medical Genetics. 18 (1): 85–92. doi:10.1515/bjmg-2015-0010. PMC 4768830. PMID 26929910...
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management, and treatment". American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184 (1): 73–80. doi:10.1002/ajmg.c.31765. ISSN 1552-4868...
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targets for intervention". American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184 (2): 428–443. doi:10.1002/ajmg.c.31807. PMC 7413625...
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true hermaphrodite with 46,XX/46,XY dispermic chimerism". Journal of Medical Genetics. 24 (12): 784–786. doi:10.1136/jmg.24.12.784. ISSN 0022-2593. PMC 1050410...
56 KB (6,558 words) - 04:39, 25 September 2024
Fraser syndrome (section Genetics)
agenesis in two consanguineous Turkish families". American Journal of Medical Genetics. 36 (4): 477–479. doi:10.1002/ajmg.1320360421. PMID 2389805. van Haelst...
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Osteogenesis imperfecta (section Genetics)
radiological, and molecular findings". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 160C (3): 175–189. doi:10.1002/ajmg.c.31334. PMID 22791419...
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Finnish heritage disease (redirect from Medical genetics of Finns)
Peltonen-Palotie Nine diseases Population genetics BCG disease outbreak in Finland in the 2000s Medical genetics of Ashkenazi Jews Finnish Association on...
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18p deletion: A genotype–phenotype correlation". American Journal of Medical Genetics Part A. 140A (11). Wiley: 1164–1171. doi:10.1002/ajmg.a.31260. ISSN 1552-4825...
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fistula, and the VACTERL association: review of genetics and epidemiology". Journal of Medical Genetics. 43 (7): 545–54. doi:10.1136/jmg.2005.038158. PMC 2564549...
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Bainbridge–Ropers syndrome (section Genetics)
correlation in the ASXL3 mutational cluster regions". European Journal of Medical Genetics. 64 (1): 104107. doi:10.1016/j.ejmg.2020.104107. PMID 33242595. S2CID 227181556...
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with further definition of a critical region". American Journal of Medical Genetics. Part A. 161A (6): 1405–1408. doi:10.1002/ajmg.a.35876. ISSN 1552-4833...
5 KB (398 words) - 14:12, 2 July 2024