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...
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| Main Authors: | , , , , , , |
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| Format: | Book |
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BMC,
2004-06-01T00:00:00Z.
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