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Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations
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  1. Correspondence to:
 Dr C Fuster, Unitat de Biologia, Facultat de Medicina, Universitat Autònoma de Barcelona, E-08193 Bellaterra, Barcelona, Spain;
 carme.fuster{at}uab.es
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Citation

Hernando C, Plaja A, Rigola MA, et al
Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations

Publication history

  • First published May 1, 2002.
Online issue publication 
May 01, 2002

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