Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.

Authors

K.C. Hoffbuhr
L.M. Moses
M.A. Jerdonek
S. Naidu
E.P. Hoffman

Document Type

Journal Article

Publication Date

2002

Journal

Mental Retardation and Development Disabilities Research Reviews

Volume

8

Issue

2

Inclusive Pages

99-105

Keywords

Pediatrics

APA Citation

Hoffbuhr, K., Moses, L., Jerdonek, M., Naidu, S., & Hoffman, E. (2002). Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.. Mental Retardation and Development Disabilities Research Reviews, 8 (2). Retrieved from https://hsrc.himmelfarb.gwu.edu/smhs_peds_facpubs/3530