Literature DB >> 13984948

Waardenburg's syndrome in father and daughter.

O THORKILGAARD.   

Abstract

Entities:  

Keywords:  DEAFNESS; EYE; FACE; GENETICS, HUMAN; PIGMENTATION DISORDERS

Mesh：

Year:  1962        PMID： 13984948     DOI： 10.1111/j.1755-3768.1962.tb07835.x

Source DB:  PubMed          Journal:  Acta Ophthalmol (Copenh)        ISSN： 0001-639X


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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

2.  Waardenburg's syndrome. Report of a family.

Authors:  J S Cant; A J Martin
Journal:  Br J Ophthalmol       Date:  1967-11       Impact factor: 4.638

Review 3.  Heterogeneity in Waardenburg syndrome.

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

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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