Wiley-Liss: American Journal of Medical Genetics Part A American Journal of Medical Genetics Part B: Neuropsychiatric Genetics American Journal of Medical 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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The American Journal of Human Genetics is a monthly peer-reviewed scientific journal in the field of human genetics. It was established in 1948 by the...
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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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"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...
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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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"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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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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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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development: cerebro-costo-mandibular syndrome or a new syndrome?". American Journal of Medical Genetics. 84 (2): 120–124. doi:10.1002/(SICI)1096-8628(19990521)8...
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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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Cohen syndrome (category Inherited disorders of trafficking)
essential features, natural history, and heterogeneity". American Journal of Medical Genetics. 102 (2): 125–35. doi:10.1002/1096-8628(20010801)102:2<125::AID-AJMG1439>3...
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Jacobsen syndrome (section Genetics)
Advances in our knowledge of phenotype and genotype". American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 169 (3): 239–250. doi:10...
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"Penta X Syndrome: A Case Report With Review of the Literature". American Journal of Medical Genetics. 40 (1): 51–56. doi:10.1002/ajmg.1320400110. PMID 1887850...
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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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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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achondroplasia in an average-sized world: An assessment of quality of life". American Journal of Medical Genetics. 120A (4): 447–458. doi:10.1002/ajmg.a.20127....
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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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CHARGE syndrome (section Genetics)
2010). "Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome". American Journal of Medical Genetics. Part A. 152A (3): 674–686. doi:10.1002/ajmg...
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overlapping 22q12.1 microdeletions involving the gene". American Journal of Medical Genetics Part A. 167 (5): 1047–1053. doi:10.1002/ajmg.a.36839. PMID 25810350...
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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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Megalencephaly (category Congenital disorders of nervous system)
of motor development. But many with megalancephaly have normal intelligence.: Delineation of a rare syndrome". American Journal of Medical Genetics Part...
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classification of joint hypermobility and related conditions". American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 175 (1): 148–157...
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of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange syndrome". American Journal of Medical Genetics....
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childhood music education and predisposition to absolute pitch". American Journal of Medical Genetics. 98 (3): 280–282. doi:10.1002/1096-8628(20010122)98:3<280::AID-AJMG1083>3...
49 KB (5,408 words) - 14:53, 15 October 2024
Lujan–Fryns syndrome (section Genetics)
"Terminal deletion of chromosome 5p in a patient with phenotypical features of Lujan-Fryns syndrome". American Journal of Medical Genetics Part A. 119A (3):...
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Proteus syndrome (redirect from Elephant man in context of NF)
"Reassessment of the Proteus syndrome literature: application of diagnostic criteria to published cases". American Journal of Medical Genetics. 130A (2):...
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Barakat syndrome (section Genetics)
Rennert, Owen M. (2018-04-16). "Barakat syndrome revisited". American Journal of Medical Genetics Part A. 176 (6): 1341–1348. doi:10.1002/ajmg.a.38693. ISSN 1552-4825...
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1996). "Familial recurrence of tracheoesophageal fistula and associated malformations". American Journal of Medical Genetics. 63 (4): 525–8. doi:10...
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XXYY syndrome (section Genetics)
2008). "A New Look at XXYY Syndrome: Medical and Psychological Features". American Journal of Medical Genetics Part A. 146A (12): 1509–22. doi:10.1002/ajmg...
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