Detalhe da pesquisa
1.
An Alu element-associated hypermethylation variant of the POMC gene is associated with childhood obesity.
PLoS Genet
; 8(3): e1002543, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22438814
2.
Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss.
Hum Mol Genet
; 17(14): 2150-9, 2008 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18407919
3.
Low prevalence of Gs alpha mutations in somatotroph adenomas of children and adolescents.
Cancer Genet Cytogenet
; 166(2): 146-51, 2006 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16631471
4.
Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation.
Lancet
; 364(9443): 1435-7, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15488219
5.
Extended clinical phenotype, endocrine investigations and functional studies of a loss-of-function mutation A150V in the thyroid hormone specific transporter MCT8.
Eur J Endocrinol
; 153(3): 359-66, 2005 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16131597
6.
Increased transactivation associated with SOX3 polyalanine tract deletion in a patient with hypopituitarism.
J Clin Endocrinol Metab
; 96(4): E685-90, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21289259