The Journal of Medical Genetics is a monthly peer-reviewed medical journal covering all aspects of medical genetics, including reviews of and opinion...
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American Journal of Medical Genetics Part A American Journal of Medical Genetics Part B: Neuropsychiatric Genetics American Journal of Medical Genetics Part...
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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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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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Nelson American Journal of Medical Genetics "AJHG Archive". "Cell Press announces new partnership with the American Society of Human Genetics" - Eurekalert...
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Ehlers–Danlos syndrome (redirect from Arthrochalasia type of Ehlers–Danlos syndrome)
international classification of the Ehlers–Danlos syndromes". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 175 (1): 8–26. doi:10...
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"Unilateral 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...
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lists academic journals that focus on the practice of medicine or any medical specialty. Journals are listed alphabetically by journal name, and also...
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"Kabuki 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...
33 KB (3,370 words) - 16:44, 31 July 2024
"Cerebrocostomandibular syndrome in four sibs, two pairs of twins". Journal of Medical Genetics. 28 (10): 704–707. doi:10.1136/jmg.28.10.704. PMC 1017059...
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Diagnosis, management, and treatment". American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184 (1): 73–80. doi:10.1002/ajmg.c.31765....
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shortly thereafter in a humorous letter to the Journal of Medical Genetics by Judith G. Hall, is a portmanteau of the words sneeze and satiation. Similar in...
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Dur O (June 2015). "Report of a new case with pentasomy X and novel clinical findings". Balkan Journal of Medical Genetics. 18 (1): 85–92. doi:10.1515/bjmg-2015-0010...
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Blackston RD, Chen AT (June 1972). "A case of 48,XXXX female with normal intelligence". Journal of Medical Genetics. 9 (2): 230–232. doi:10.1136/jmg.9.2.230...
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The European Journal of Medical Genetics is a monthly peer-reviewed medical journal covering medical genetics in human and experimental systems. It was...
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"Behavioral phenotype of 49,XXXXY syndrome: Presence of anxiety-related symptoms and intact social awareness". American Journal of Medical Genetics. 182 (5): 974–986...
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XX male syndrome (redirect from 46,XX testicular disorders of sex development)
2020). "The epidemiology of sex chromosome abnormalities". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 184 (2): 202–215. doi:10...
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Brachydactyly type D (section Genetics)
"Symphalangism with multiple anomalies of the hands and feet: A new genetic trait". American Journal of Medical Genetics. 10 (3): 245–55. doi:10.1002/ajmg...
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molecular characterization of individuals with 18p deletion: A genotype–phenotype correlation". American Journal of Medical Genetics Part A. 140A (11). Wiley:...
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(2020). "The epidemiology of sex chromosome abnormalities". American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184 (2): 202–215. doi:10...
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Phocomelia (category Congenital disorders of musculoskeletal system)
Phocomelia Spectrum - A Case Report of an Adult With Review of the Literature" (PDF). American Journal of Medical Genetics. 152: 472=478. Retrieved 2023-04-25...
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Marfan syndrome (category Disorders of fascia)
variant of Marfan syndrome with congenital lipodystrophy results from mutations at the 3' end of FBN1 gene". European Journal of Medical Genetics. 57 (5):...
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Blaschko's lines (redirect from Lines of Blaschko)
Kamlesh (2020-09-01). "Natural human chimeras: A review". European Journal of Medical Genetics. 63 (9): 103971. doi:10.1016/j.ejmg.2020.103971. ISSN 1769-7212...
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Pycnodysostosis (section Genetics)
genotypic spectrum of CTSK variants in a cohort of twenty-five Indian patients with pycnodysostosis". European Journal of Medical Genetics. 64 (7): 104235...
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Osteogenesis imperfecta (category CS1 maint: DOI inactive as of September 2024)
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...
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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....
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Beckwith–Wiedemann syndrome (section Genetics)
(hemihypertrophy): report of a prospective multicenter study of the incidence of neoplasia and review". American Journal of Medical Genetics. 79 (4): 274–8. doi:10...
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Treacher Collins syndrome (category Congenital disorders of musculoskeletal system)
Prenatal diagnosis of micrognathia in 41 fetuses: Retrospective analysis of outcome and genetic etiologies. American Journal of Medical Genetics Part A, 179(12)...
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Holoprosencephaly (category Congenital disorders of nervous system)
maxillary central incisor: a study of 13 patients and review of the literature". American Journal of Medical Genetics. 102 (1): 1–10. doi:10...
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Clinical Genetics is a monthly peer-reviewed medical journal covering medical genetics. It was established in 1970 and is published by Wiley-Blackwell...
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