Literature DB >> 14017880

Waardenburg's syndrome.

J CALINIKOS.   

Abstract

Entities:  

Keywords:  DEAF-MUTISM; EYE; PIGMENTATION DISORDERS

Mesh：

Year:  1963        PMID： 14017880     DOI： 10.1017/s0022215100060369

Source DB:  PubMed          Journal:  J Laryngol Otol        ISSN： 0022-2151            Impact factor:   1.469


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  4 in total

1.  Waardenburg syndrome (WS): the analysis of a single family with a WS1 mutation showing linkage to RFLP markers on human chromosome 2q.

Authors:  J H Asher; R Morell; T B Friedman
Journal:  Am J Hum Genet       Date:  1991-01       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.  Waardenburg's memorial lecture: Waardenburg's syndrome.

Authors:  J François
Journal:  Int Ophthalmol       Date:  1982-05       Impact factor: 2.031

4.  WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION.

Authors:  M W PARTINGTON
Journal:  Can Med Assoc J       Date:  1964-04-25       Impact factor: 8.262
  4 in total

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