Literature DB >> 7180872

Familial omphalocele: analysis of risk factors and case report.

J H DiLiberti.   

Abstract

Mesh：

Year:  1982        PMID： 7180872     DOI： 10.1002/ajmg.1320130306

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  2 in total

1.  Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele.

Authors:  Uppala Radhakrishna; Swapan K Nath; Ken McElreavey; Uppala Ratnamala; Celi Sun; Amit K Maiti; Maryline Gagnebin; Frédérique Béna; Heather L Newkirk; Andrew J Sharp; David B Everman; Jeffrey C Murray; Charles E Schwartz; Stylianos E Antonarakis; Merlin G Butler
Journal:  J Med Genet       Date:  2012-04       Impact factor: 6.318

2.  Familial omphalocele.

Authors:  K Steele; N C Nevin
Journal:  Ulster Med J       Date:  1985-10
  2 in total

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