Literature DB >> 13788154

Syndrome of Waardenburg with deafness.

S ZELIG.   

Abstract

Entities:  

Keywords:  DEAFNESS/genetics; EYE/abnormalities; HAIR; PIGMENTATION DISORDERS/genetics

Mesh：

Year:  1961        PMID： 13788154     DOI： 10.1288/00005537-196101000-00002

Source DB:  PubMed          Journal:  Laryngoscope        ISSN： 0023-852X            Impact factor:   3.325


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  4 in total

1.  WAARDENBURG'S SYNDROME: REPORT OF A PEDIGREE.

Authors:  A C HANSEN; G ACKAOUY; E P CRUMP
Journal:  J Natl Med Assoc       Date:  1965-01       Impact factor: 1.798

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 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.  Degeneration of saccular hair cells caused by MITF gene mutation.

Authors:  Yi Du; Li-Li Ren; Qing-Qing Jiang; Xing-Jian Liu; Fei Ji; Yue Zhang; Shuo-Long Yuan; Zi-Ming Wu; Wei-Wei Guo; Shi-Ming Yang
Journal:  Neural Dev       Date:  2019-01-11       Impact factor: 3.842
  4 in total

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