Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: PHF8[original query] |
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Autism-associated familial microdeletion of Xp11.22. Clinical genetics 2008 Aug 74 (2): 134-44. Qiao Y, Liu X, Harvard C, Hildebrand M J, Rajcan-Separovic E, Holden J J A, Lewis M E |
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE. Translational psychiatry 2012 2 e179. Nava C, Lamari F, Héron D, Mignot C, Rastetter A, Keren B, Cohen D, Faudet A, Bouteiller D, Gilleron M, Jacquette A, Whalen S, Afenjar A, Périsse D, Laurent C, Dupuits C, Gautier C, Gérard M, Huguet G, Caillet S, Leheup B, Leboyer M, Gillberg C, Delorme R, Bourgeron T, Brice A, Depienne |
Application of high-resolution array platform for genome-wide copy number variation analysis in patients with nonsyndromic cleft lip and palate. Journal of clinical laboratory analysis 2018 3 32 (6): e22428. da Silva Heglayne Pereira Vital, Oliveira Gustavo Henrique de Medeiros, Ururahy Marcela Abbott Galvão, Bezerra João Felipe, de Souza Karla Simone Costa, Bortolin Raul Hernandes, Luchessi André Ducati, Silbiger Vivian Nogueira, Lima Valéria Morgiana Gualberto Duarte Moreira, Leite Gisele Correia Pacheco, Brito Maria Edinilma Felinto, Ribeiro Erlane Marques, Gil-da-Silva-Lopes Vera Lúcia, de Rezende Adriana Augus |
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