A carregar...

Prader-Willi Syndrome: Clinical and Genetic Findings

Since the initial medical description by Prader, Labhart and Willi in 1956 of individuals with overlapping features, the Prader-Willi syndrome has become recognized as a classical but sporadic genetic syndrome. Prader-Willi syndrome is the most common genetic cause of life-threatening obesity in hum...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Endocrinologist
Main Authors: Butler, Merlin G., Thompson, Travis
Formato: Artigo
Idioma:Inglês
Publicado em: 2000
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4996620/
https://ncbi.nlm.nih.gov/pubmed/27570435
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!