Literature DB >> 14018109

Waardenbrug's syndrome. A variation of the first arch syndrome.

B CAMPBELL, N R CAMPBELL.   

Abstract

Entities:  

Keywords:  DEAF-MUTISM; OPHTHALMOLOGY

Mesh：

Year:  1962        PMID： 14018109     DOI： 10.1001/archderm.1962.01590120016003

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN： 0003-987X


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  6 in total

Review 1.  PROFOUND CHILDHOOD DEAFNESS.

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

2.  Waardenburg syndrome: A rare case with bilateral congenital cataract: An unusual entity.

Authors:  Nitin Vichare; N Bhargava
Journal:  Med J Armed Forces India       Date:  2012-12-01

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 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

Review 6.  Genetic insights, disease mechanisms, and biological therapeutics for Waardenburg syndrome.

Authors:  Sida Huang; Jian Song; Chufeng He; Xinzhang Cai; Kai Yuan; Lingyun Mei; Yong Feng
Journal:  Gene Ther       Date:  2021-02-25       Impact factor: 4.184
  6 in total

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