Molecular characterization of patients with 18q23 deletions.

The 18q- syndrome is a deletion syndrome that is characterized by mental retardation, hearing loss, midfacial hypoplasia, growth deficiency, and limb anomalies. Most patients with this syndrome have deletions from 18q21-qter. We report on three patients with deletions of 18q23. A mother and daughter...

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Bibliographic Details
Main Authors: Strathdee, G, Sutherland, R, Jonsson, J J, Sataloff, R, Kohonen-Corish, M, Grady, D, Overhauser, J
Format: Artigo
Language:Inglês
Published: 1997
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1712465/
https://ncbi.nlm.nih.gov/pubmed/9106532
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