Literature DB >> 21910236

Inherited interstitial 16q21 deletion of 5.8 Mb without apparent phenotypic effect in three generations of a family: an array-CGH study.

Aurélie Coussement1, Philippe Lochu, Jean-Michel Dupont, Agnès Choiset.   

Abstract

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Year:  2011        PMID: 21910236     DOI: 10.1002/ajmg.a.34210

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


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  1 in total

1.  Pure 16q21q22.1 deletion in a complex rearrangement possibly caused by a chromothripsis event.

Authors:  Rita Genesio; Valentina Ronga; Pia Castelluccio; Gennaro Fioretti; Angela Mormile; Graziella Leone; Anna Conti; Maria Luigia Cavaliere; Lucio Nitsch
Journal:  Mol Cytogenet       Date:  2013-08-01       Impact factor: 2.009

  1 in total

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