RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37.

Albright hereditary osteodystrophy (AHO) is an autosomal dominant disorder characterised by the presence of brachymetaphalangism, short stature, obesity, and mental retardation. Variable biochemical changes many represent either pseudohypoparathyroidism (PHP) owing to resistance to parathormone (PTH...

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Detalhes bibliográficos
Main Authors: Power, M M, James, R S, Barber, J C, Fisher, A M, Wood, P J, Leatherdale, B A, Flanagan, D E, Hatchwell, E
Formato: Artigo
Idioma:Inglês
Publicado em: 1997
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050913/
https://ncbi.nlm.nih.gov/pubmed/9138150
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