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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: May 29, 2023. (Total: 217385Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Rett Syndrome and FRAXA[original query]
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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