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Interstitial 6q deletion: clinical and array CGH characterisation of a new patient

✍ Scribed by Cédric Le Caignec; Ann Swillen; Elvire Van Asche; Jean-Pierre Fryns; Joris R. Vermeesch


Book ID
116432798
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
221 KB
Volume
48
Category
Article
ISSN
1769-7212

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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