Literature DB >> 13434603

Omphalocele in siblings; report of two cases with surgical recovery.

R E ROTHENBERG.   

Abstract

Keywords:  HERNIA, UMBILICAL/in infant and child

Mesh：

Year:  1957        PMID： 13434603

Source DB:  PubMed          Journal:  AMA Arch Surg        ISSN： 0096-6908


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  5 in total

1.  Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome.

Authors:  D Viljoen; R Ramesar
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

2.  Familial occurrence of omphalocele.

Authors:  H D Rott; H Truckenbrodt
Journal:  Humangenetik       Date:  1974

3.  Omphalocele affecting both members of a twin pregnancy.

Authors:  A A Yuzpe; H D Johnson
Journal:  Can Med Assoc J       Date:  1968 Aug 24-31       Impact factor: 8.262

4.  Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases.

Authors:  A L Kosseff; J Herrmann; E F Gilbert; C Viseskul; M Lubinsky; J M Opitz
Journal:  Eur J Pediatr       Date:  1976-10-01       Impact factor: 3.183

5.  Etiological study of omphalocele.

Authors:  A Czeizel; M Vitéz
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
  5 in total

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