Literature DB >> 1270082

Exomphalos and trisomy 18 syndrome. Report of two cases.

J Zizka, P Balícek, E Pokorná, K Dostalíková, M Kodousková.   

Abstract

A large exomphalose was found in two infants with a clinically and cytogenetically typical picture of trisomy 18 syndrome. In addition one infant was a case of male pseudohermaphroditism.

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Year:  1976        PMID： 1270082     DOI： 10.1007/BF00291509

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  4 in total

1.  A PROBABLE 17-18 TRISOMY SYNDROME WITH PHOCOMELIA, EXOMPHALOS, AND AGENESIS OF HEMIDIAPHRAGM.

Authors:  T KAJII; K OIKAWA; K ITAKURA; T OHSAWA
Journal:  Arch Dis Child       Date:  1964-10       Impact factor: 3.791

2.  Chromosome examination of newborn children: purpose and ethical aspects.

Authors:  J Nielsen
Journal:  Humangenetik       Date:  1975

3.  Study of selected congenital anomalies in Pennsylvania.

Authors:  H B Bock; J H Zimmerman
Journal:  Public Health Rep       Date:  1967-05       Impact factor: 2.792

4.  Structural abnormalities of chromosome 18. II. Two familial translocations, B-18 and 16-18, ascertained through unbalanced forms.

Authors:  B Eriksson; M Fraccaro; M Hultén; J Lindsten; C Thorén; L Tiepolo
Journal:  Ann Genet       Date:  1971-12
  4 in total
  1 in total

1.  Omphalocele and partial trisomy 1q syndrome.

Authors:  H Chen; J J Gershanik; J B Mailhes; I D Sanusi
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132
  1 in total

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