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Subtelomeric 6p deletion: Clinical and array-CGH characterization in two patients

✍ Scribed by Danielle Martinet; Isabel Filges; Nathalie Besuchet Schmutz; Michael A. Morris; Anne-Claude Gaide; Sophie Dahoun; Armand Bottani; Marie-Claude Addor; Stylianos E. Antonarakis; Jacques S. Beckmann; Frédérique Béna


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
227 KB
Volume
146A
Category
Article
ISSN
1552-4825

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Array-CGH and clinical characterization
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## Abstract Subtelomeric terminal 6p deletion has been recognized as a clinically identifiable syndrome including facial dysmorphism, malformation of the anterior eye chamber, hearing loss, heart defects, and developmental delay. Genotype–phenotype correlations of previously published patients have