Literature DB >> 3308683

Split hand, obstructive urinary anomalies and spina bifida or diaphragmatic defect syndrome with autosomal dominant inheritance.

A Czeizel1, A Losonci.   

Abstract

Three members of a nuclear family were affected by split hands and feet or syndactyly, obstructive urinary anomalies and spina bifida or diaphragmatic defect.

Entities:  

Mesh：

Year:  1987        PMID： 3308683     DOI： 10.1007/BF00272395

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


  2 in total

1.  A new variant of the acrorenal syndrome associated with bilateral oligomeganephronic hypoplasia.

Authors:  M Miltényi; L Balogh; K Schmidt; Z Detre; T Hernády; A Czeizel
Journal:  Eur J Pediatr       Date:  1984-04       Impact factor: 3.183

2.  A family study of congenital diaphragmatic defects.

Authors:  A Czeizel; M Kovács
Journal:  Am J Med Genet       Date:  1985-05
  2 in total
  3 in total

1.  Epidemiological study of congenital diaphragmatic defects with special reference to aetiology.

Authors:  N Philip; D Gambarelli; J M Guys; J Camboulives; S Ayme
Journal:  Eur J Pediatr       Date:  1991-08       Impact factor: 3.183

Review 2.  Spina Bifida: Pathogenesis, Mechanisms, and Genes in Mice and Humans.

Authors:  Siti W Mohd-Zin; Ahmed I Marwan; Mohamad K Abou Chaar; Azlina Ahmad-Annuar; Noraishah M Abdul-Aziz
Journal:  Scientifica (Cairo)       Date:  2017-02-13

3.  Posterior axis formation requires Dlx5/Dlx6 expression at the neural plate border.

Authors:  Nicolas Narboux-Neme; Marc Ekker; Giovanni Levi; Eglantine Heude
Journal:  PLoS One       Date:  2019-03-19       Impact factor: 3.240
  3 in total

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