Literature DB >> 14124244

WAARDENBURG'S SYNDROME WITH DEAFNESS AS THE PRESENTING SYMPTOM. REPORT OF TWO CASES.

N I HOUGHTON.   

Abstract

Keywords:  ABNORMALITIES; CHILD; DEAFNESS; EYEBROWS; EYELIDS; GENETICS, HUMAN; HAIR; IRIS

Mesh：

Year:  1964        PMID： 14124244

Source DB:  PubMed          Journal:  N Z Med J        ISSN： 0028-8446


× No keyword cloud information.
  3 in total

Review 1.  PROFOUND CHILDHOOD DEAFNESS.

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

Review 2.  Inherited diseases of the inner ear in man in the light of studies on the mouse.

Authors:  M S Deol
Journal:  J Med Genet       Date:  1968-06       Impact factor: 6.318

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
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.