A carregar...
Growth Hormone Receptor (GHR) Gene Polymorphism and Prader-Willi Syndrome
Prader-Willi syndrome (PWS) is a genomic imprinting disorder due to loss of paternally expressed genes in the 15q11-q13 region and characterized by hypotonia, a poor suck, failure to thrive, hypogonadism/hypogenitalism, growth hormone deficiency, learning and behavioral problems and hyperphagia lead...
Na minha lista:
| Main Authors: | , , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3689873/ https://ncbi.nlm.nih.gov/pubmed/23696513 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.35980 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|