Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: Rare association with pulmonary valve stenosis-Reference-Cited by-同舟云学术

Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: Rare association with pulmonary valve stenosis

Published:2013-03 Issue:3 Volume:56 Page:144-149
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Digilio M. Cristina,Bernardini Laura,Consoli Federica,Lepri Francesca R.,Giuffrida M. Grazia,Baban Anwar,Surace Cecilia,Ferese Rosangela,Angioni Adriano,Novelli Antonio,Marino Bruno,De Luca Alessandro,Dallapiccola Bruno

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference23 articles.

1. Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes;Mefford;N. Engl. J. Med.,2008

2. Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities;Brunetti-Pierri;Nat. Genet.,2008

3. Duplication hotspots, rare genomic disorders, and common disease;Mefford;Curr. Opin. Genet. Dev.,2009

4. Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease;Christiansen;Circ. Res.,2004

5. BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1;Brunet;BMC Med. Genet.,2009

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