Absence of learning difficulties in a hyperactive boy with a terminal Xp deletion encompassing the MRX49locus

Clinical and molecular studies undertaken over the past 10 years on patients with distal Xp deletions imply, however, that the putative X linked mental retardation (XLMR) gene,MRX49, lies distal toGS1 and STS but proximal to DXS31 and CDPX1 (fig 1 ).

Saved in:
Bibliographic Details
Published in:Journal of medical genetics 2001-07, Vol.38 (7), p.466
Main Authors: Tobias, E S, Bryce, G, Farmer, G, Barton, J, Colgan, J, Morrison, N, Cooke, A, Tolmie, J L
Format: Article
Language:English
Subjects:
Attention Deficit Hyperactivity Disorder
Chromosomes
Genes
Hyperactivity
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Clinical and molecular studies undertaken over the past 10 years on patients with distal Xp deletions imply, however, that the putative X linked mental retardation (XLMR) gene,MRX49, lies distal toGS1 and STS but proximal to DXS31 and CDPX1 (fig 1 ).
ISSN:0022-2593
1468-6244
DOI:10.1136/jmg.38.7.466