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

• Main Authors: Ritch Robert (Author), Munier Francis (Author), Addison Mark K (Author), Jaafar Mohamad S (Author), Gould Douglas B (Author), MacDonald Ian M (Author), Walter Michael A (Author)
• Format: Book
• Published: BMC, 2004-06-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

<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...