Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia-Reference-Cited by-同舟云学术

Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia

Published:2011-01-12 Issue:5 Volume:19 Page:602-606
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Cognet Marie,Nougayrede Agnés,Malan Valérie,Callier Patrick,Cretolle Celia,Faivre Laurence,Genevieve David,Goldenberg Alice,Heron Delphine,Mercier Sandra,Philip Nicole,Sigaudy Sabine,Verloes Alain,Sarnacki Sabine,Munnich Arnold,Vekemans Michel,Lyonnet Stanislas,Etchevers Heather,Amiel Jeanne,Pontual Loïc de

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2010225.pdf

Reference14 articles.

1. Feingold M : Case report 30. Synd Ident 1975; 3: 16–17.

2. Celli J, van Beusekom E, Hennekam RC et al: Familial syndromic esophageal atresia maps to 2p23-p24. Am J Hum Genet 2000; 66: 436–444.

3. van Bokhoven H, Celli J, van Reeuwijk J et al: MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome. Nat Genet 2005; 37: 465–467.

4. Marcelis CL, Hol FA, Graham GE et al: Genotype-phenotype correlations in MYCN-related Feingold syndrome. Hum Mutat 2008; 29: 1125–1132.

5. Brodeur GM, Seeger RC, Schwab M, Varmus HE, Bishop JM : Amplification of N-myc in untreated human neuroblastomas correlates with advanced disease stage. Science 1984; 224: 1121–1124.

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