Literature DB >> 6842346

Waardenburg and Hirschsprung syndromes.

L M Ambani.   

Abstract

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Year:  1983        PMID： 6842346     DOI： 10.1016/s0022-3476(83)80267-4

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  6 in total

1.  Mouse and hamster mutants as models for Waardenburg syndromes in humans.

Authors:  J H Asher; T B Friedman
Journal:  J Med Genet       Date:  1990-10       Impact factor: 6.318

2.  Exclusion of RET and Pax 3 loci in Waardenburg-Hirschsprung disease.

Authors:  T Attié; M Till; A Pelet; P Edery; J P Bonnet; A Munnich; S Lyonnet
Journal:  J Med Genet       Date:  1995-04       Impact factor: 6.318

3.  Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.

Authors:  L A Farrer; K M Grundfast; J Amos; K S Arnos; J H Asher; P Beighton; S R Diehl; J Fex; C Foy; T B Friedman
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

4.  Long segment Hirschsprung's disease in the Waardenburg-Shah syndrome.

Authors:  E J Gnananayagam; R Solomon; A Chandran; S Anbarasi; S Sen; P D Moses
Journal:  Pediatr Surg Int       Date:  2003-06-14       Impact factor: 1.827

Review 5.  Intestinal aganglionosis associated with the Waardenburg syndrome: report of two cases and review of the literature.

Authors:  Fumiaki Toki; Norio Suzuki; Ken Inoue; Makoto Suzuki; Kyoko Hirakata; Kyoko Nagai; Minoru Kuroiwa; James R Lupski; Yoshiaki Tsuchida
Journal:  Pediatr Surg Int       Date:  2003-12-23       Impact factor: 1.827

6.  Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.

Authors:  G Van Camp; M N Van Thienen; I Handig; B Van Roy; V S Rao; A Milunsky; A P Read; C T Baldwin; L A Farrer; M Bonduelle
Journal:  J Med Genet       Date:  1995-07       Impact factor: 6.318
  6 in total

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