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Clinical Genetics|September 13, 2006
Germline mosaicism for a MECP2 mutation in a man with two Rett daughtersJ C Evans, H L Archer, S D Whatley, et al.Journal of Intellectual Disability Research : JIDR|April 25, 2006
People with MECP2 mutation-positive Rett disorder who converseA M Kerr, H L Archer, J C Evans, et al.Journal of Medical Genetics|April 14, 2006
CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patientsH L Archer, J Evans, S Edwards, et al.American Journal of Medical Genetics. Part A|June 7, 2005
Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pterH L Archer, S Gupta, S Enoch, et al.Journal of Medical Genetics|September 27, 2005
Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patientsH L Archer, S D Whatley, J C Evans, et al.Pageof 1