Literature DB >> 6467668

Prader-Willi syndrome in black females.

W L Golden, J M Hanchett, N Breslin, M W Steele.   

Abstract

Reports of Black females with Prader-Willi have been rare. This communication describes two Black females with Prader-Willi syndrome. Chromosome analysis revealed a small deletion of the proximal portion of a chromosome 15 in one case and apparently normal chromosomes in the other.

Entities:  

Mesh:

Year:  1984        PMID: 6467668     DOI: 10.1111/j.1399-0004.1984.tb00807.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  3 in total

1.  Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome.

Authors:  M G Butler; F J Meaney; C G Palmer
Journal:  Am J Med Genet       Date:  1986-03

2.  Prader-Willi syndrome: current understanding of cause and diagnosis.

Authors:  M G Butler
Journal:  Am J Med Genet       Date:  1990-03

3.  Syndromes, communicative disorders, and black children.

Authors:  M D Meyerson; G T Weddington
Journal:  J Natl Med Assoc       Date:  1986-05       Impact factor: 1.798

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.