Literature DB >> 5085935

Waardenburg's syndrome in two siblings, both parents and their maternal grandmother.

T J David, R P Warin.   

Abstract

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Year:  1972        PMID： 5085935      PMCID： PMC1644228     

Source DB:  PubMed          Journal:  Proc R Soc Med        ISSN： 0035-9157


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  2 in total

1.  Studies on Spotting Patterns. IV. Pattern Variation and Its Developmental Significance.

Authors:  D R Charles
Journal:  Genetics       Date:  1938-11       Impact factor: 4.562

2.  [A Swiss family with Klein-Waardenburg's syndrome associated with hyperkeratosis of the palms and feet and with serious oligophrenia].

Authors:  S Amini-Elihou
Journal:  J Genet Hum       Date:  1970-12
  2 in total
  3 in total

1.  Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse.

Authors:  C Foy; V Newton; D Wellesley; R Harris; A P Read
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

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.  Hypomelanosis of Itô: a neurocutaneous syndrome.

Authors:  T J David
Journal:  Arch Dis Child       Date:  1981-10       Impact factor: 3.791
  3 in total

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