Literature DB >> 4095814

Familial omphalocele.

K Steele, N C Nevin.   

Abstract

Mesh：

Year:  1985        PMID： 4095814      PMCID： PMC2448112     

Source DB:  PubMed          Journal:  Ulster Med J        ISSN： 0041-6193


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  3 in total

1.  Four cases of omphalocele in two generations of the same family.

Authors:  A Osuna; S Lindham
Journal:  Clin Genet       Date:  1976-03       Impact factor: 4.438

2.  Familial occurrence of omphalocele suggesting sex-linked inheritance.

Authors:  S Havalad; H Noblett; B D Speidel
Journal:  Arch Dis Child       Date:  1979-02       Impact factor: 3.791

3.  Familial omphalocele: analysis of risk factors and case report.

Authors:  J H DiLiberti
Journal:  Am J Med Genet       Date:  1982-11
  3 in total
  1 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
  1 in total

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