Affiliation: Alfred I. duPont Hospital for Children
- Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndromeCarolyn Schanen
Nemours Biomedical Research, Alfred I duPont Hospital for Children, Room H3B 337, PO Box 269, Wilmington, DE 19899, USA
Am J Med Genet A 126:129-40. 2004..These results emphasize the limitations of such analyses in larger mutation groups, either by type or position...
- The phenotypic consequences of MECP2 mutations extend beyond Rett syndromeSara Hammer
Departments of Human Genetics, Mental Retardation Research Center, University of California, Los Angeles, 695 Chales Young Drive South, Los Angeles California, USA
Ment Retard Dev Disabil Res Rev 8:94-8. 2002..Thus, because of the range of disparate phenotypes, the gene may account for a relatively large portion of mental retardation in the population...
- Neural, not gonadal, origin of brain sex differences in a gynandromorphic finchRobert J Agate
Department of Physiological Science, University of California, Los Angeles, CA 90095, USA
Proc Natl Acad Sci U S A 100:4873-8. 2003..Because both sides of the song circuit were more masculine than that of females, diffusible factors such as hormones of gonadal or neural origin also likely played a role in sexual differentiation...