The clinical variability of the MECP2 duplication syndrome: description of two families with duplications excluding L1CAM and FLNA

Saved in:

Bibliographic Details
Published in:	Clinical genetics Vol. 75; no. 3; pp. 301 - 303
Main Authors:	Kirk, EP, Malaty-Brevaud, V, Martini, N, Lacoste, C, Levy, N, Maclean, K, Davies, L, Philip, N, Badens, C
Format:	Journal Article
Language:	English
Published:	Oxford, UK Blackwell Publishing Ltd 01-03-2009
Subjects:	Adult Child Chromosomes, Human, X - genetics Contractile Proteins - genetics Family Female Filamins Gene Duplication Humans Male Mental Retardation, X-Linked - diagnosis Mental Retardation, X-Linked - genetics Methyl-CpG-Binding Protein 2 - genetics Microfilament Proteins - genetics Neural Cell Adhesion Molecule L1 - genetics Syndrome
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Description
Bibliography:	istex:20F00DC01FA6C6418243964B22BDC6696F420BB8 ark:/67375/WNG-TKN55HT4-T ArticleID:CGE1102 SourceType-Other Sources-1 ObjectType-Article-2 content type line 63 ObjectType-Correspondence-1
ISSN:	0009-9163 1399-0004
DOI:	10.1111/j.1399-0004.2008.01102.x