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Sequence variants within exon 1 of MECP2 occur in females with mental retardation. Am J Medical Genetics Part B (Neuropsychiatric Genetic) 144B:355–360 (2007)
Author(s) -
Harvey Chris G.,
Me Sailesh D.,
Stachowiak Beata,
Noor Abdul,
Proctor Adam,
Mensah Albert K.,
Mnatzakanian Gevork N.,
Alfred Simon E.,
Guo Ray,
Scherer Stephen W.,
Kennedy James L.,
Roberts Wendy,
Srivastava Anand K.,
Minassian Berge A.,
Vincent John B.
Publication year - 2007
Publication title -
american journal of medical genetics part b: neuropsychiatric genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.393
H-Index - 126
eISSN - 1552-485X
pISSN - 1552-4841
DOI - 10.1002/ajmg.b.30627
Subject(s) - genetics , medical genetics , mecp2 , exon , biology , sequence (biology) , gene , phenotype