Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and FGD1[original query] |
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Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 gene. American journal of medical genetics. Part A 2010 1 152A (2): 313-8. Orrico A, Galli L, Faivre L, Clayton-Smith J, Azzarello-Burri S M, Hertz J M, Jacquemont S, Taurisano R, Arroyo Carrera I, Tarantino E, Devriendt K, Melis D, Thelle T, Meinhardt U, Sorrentino |
No association between FGD1 gene polymorphisms and intellectual developmental disability in the Qinba mountain area. Genetics and molecular research : GMR 2014 13 (1): 127-33. Li J L, Li Y J, Zhang K J, Lan L, Shi J G, Yang X, Zhang M J, Zhang F C, Gao X |
Xp11.22 duplications in four unrelated Chinese families: delineating the genotype-phenotype relationship for HSD17B10 and FGD1. BMC medical genomics 2020 5 13 (1): 66. Wang Qingming, Chen Pengliang, Liu Jianxin, Lou Jiwu, Liu Yanhui, Yuan Haimi |
The Prevalence of Clinical Features in Patients with Aarskog-Scott Syndrome and Assessment of Genotype-Phenotype Correlation: A Systematic Review. Genetics research 2021 3 2021 6652957. Zanetti Drumond Victor, Sousa Salgado Lucas, Sousa Salgado Camila, Oliveira Vitor Augusto de Lima, de Assis Eliene Magda, Campos Ribeiro Michel, Furtado Valadão Analina, Orrico Alfre |
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