Literature DB >> 5310696

[Waardenburg's syndrome. A familial case relating to 4 generations and 23 individuals].

C Roux, G Baheux, M Gaulier, R Caldera, L Soepardan.   

Abstract

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Year:  1970        PMID： 5310696

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  3 in total

Review 1.  Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans.

Authors:  C E Moase; D G Trasler
Journal:  J Med Genet       Date:  1992-03       Impact factor: 6.318

Review 2.  Heterogeneity in Waardenburg syndrome.

Authors:  M J Hageman; J W Delleman
Journal:  Am J Hum Genet       Date:  1977-09       Impact factor: 11.025

3.  Possible Waardenburg syndrome with gastrointestinal anomalies.

Authors:  J Nutman; R Steinherz; Y Sivan; R M Goodman
Journal:  J Med Genet       Date:  1986-04       Impact factor: 6.318
  3 in total

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