Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Rett Syndrome and FRAXA[original query] |
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MECP2 mutations or polymorphisms in mentally retarded boys: diagnostic implications. Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology 2003 7 (1): 3-7. Bourdon Violaine, Philippe Christophe, Martin Dominique, Verloès Alain, Grandemenge Agnès, Jonveaux Philip |
Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation. European journal of medical genetics 0 50 (3): 200-8. Lesca Gaëtan, Bernard Virginie, Bozon Muriel, Touraine Renaud, Gérard Daniel, Edery Patrick, Calender Ala |
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- Page last updated:May 22, 2023
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