Literature DB >> 13650669

An English family with Waardenburg's syndrome.

M W PARTINGTON.   

Abstract

Entities:  

Keywords:  DEAF-MUTISM/heredity; EYE/abnormalities

Mesh：

Year:  1959        PMID： 13650669      PMCID： PMC2012350          DOI： 10.1136/adc.34.174.154

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  4 in total

1.  The first arch syndrome.

Authors:  J McKENZIE
Journal:  Arch Dis Child       Date:  1958-10       Impact factor: 3.791

2.  [Deaf-mutism with Waardenburg-Klein syndrome in children].

Authors:  L S WILDERVANCK
Journal:  Ned Tijdschr Geneeskd       Date:  1957-06-15

3.  [A new form of congenital hereditary deafness (Waardenburg's syndrome)].

Authors:  D P R KEIZER
Journal:  Ned Tijdschr Geneeskd       Date:  1952-10-11

4.  A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.

Authors:  P J WAARDENBURG
Journal:  Am J Hum Genet       Date:  1951-09       Impact factor: 11.025
  4 in total
  5 in total

1.  Waardenburg's syndrome in a girl.

Authors:  M L Magotra; O P Katira; V R Anand
Journal:  Indian J Pediatr       Date:  1975-02       Impact factor: 1.967

Review 2.  PROFOUND CHILDHOOD DEAFNESS.

Authors:  G R FRASER
Journal:  J Med Genet       Date:  1964-12       Impact factor: 6.318

3.  Waardenburg's syndrome and familial periodic paralysis.

Authors:  C H Tay
Journal:  Postgrad Med J       Date:  1971-06       Impact factor: 2.401

Review 4.  Heterogeneity in Waardenburg syndrome.

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

5.  Waardenburg's memorial lecture: Waardenburg's syndrome.

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

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