Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: Relevance to ocular dysgenesis and hearing impairment

Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: Relevance to ocular dysgenesis and hearing impairment

<p>Abstract</p> <p>Background</p> <p>Thirty-nine patients have been described with deletions involving chromosome 6p25. However, relatively few of these deletions have had molecular characterization. Common phenotypes of 6p25 deletion syndrome patients include hydroceph...

Full description

Bibliographic Details
Main Authors: Ritch Robert, Munier Francis, Addison Mark K, Jaafar Mohamad S, Gould Douglas B, MacDonald Ian M, Walter Michael A
Format: Article
Language:English
Published: BMC 2004-06-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/5/17

Similar Items

Similar Items