Genotype-phenotype correlations in MYCN-related Feingold syndrome-Reference-Cited by-同舟云学术

Genotype-phenotype correlations in MYCN-related Feingold syndrome

Published:2008-09 Issue:9 Volume:29 Page:1125-1132
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Marcelis Carlo L.M.,Hol Frans A.,Graham Gail E.,Rieu Paul N.M.A.,Kellermayer Richard,Meijer Rowdy P.P.,Lugtenberg Dorien,Scheffer Hans,van Bokhoven Hans,Brunner Han G.,de Brouwer Arjan P.M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference32 articles.

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3. Familial syndromic esophageal atresia maps to 2p23-p24;Celli;Am J Hum Genet,2000

4. Feingold syndrome: clinical review and genetic mapping;Celli;Am J Med Genet A,2003

5. Identification of N-myc regulatory regions involved in embryonic expression;Charron;Pediatr Res,2002

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