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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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Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations

Authors

  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
Journal of Medical Genetics 2002;39:e24.

Publication history

  • First published May 1, 2002.
Online issue publication 
April 27, 2016

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Copyright 2002 Journal of Medical Genetics