8p23.1 duplication detected by array-CGH with complete atrioventricular septal defect and unilateral hand preaxial hexadactyly
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
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3. Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level;Barber;Eur J Hum Genet,2005
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