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Clinical epigenetics, ISSN 1868-7083, 11/2018, Volume 10, Issue 1, pp. 146 - 18
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 06/2013, Volume 368, Issue 26, pp. 2467 - 2475
Journal Article
Journal of Clinical Endocrinology and Metabolism, ISSN 0021-972X, 05/2017, Volume 102, Issue 5, pp. 1557 - 1567
Journal Article
Journal of Clinical Endocrinology and Metabolism, ISSN 0021-972X, 06/2019, Volume 104, Issue 6, pp. 2112 - 2120
Delta-like homolog 1 (DLK1), also called preadipocyte factor 1, prevents adipocyte differentiation and has been considered a molecular gatekeeper of... 
Journal Article
Neuroendocrinology, ISSN 0028-3835, 09/2018, Volume 107, Issue 2, pp. 127 - 132
Context: Loss-of-function mutations in the coding region of MKRN3, a maternally imprinted gene at chromosome 15q11.2, are a common cause of familial central... 
Original Paper | Genetic alteration | MKRN3 promoter region | Regulatory region | Central precocious puberty | PRADER-WILLI | TRANSCRIPTION | IMPRINTED GENE MKRN3 | NEUROSCIENCES | RING | ENDOCRINOLOGY & METABOLISM | MUTATIONS | EXPRESSION | DREAM PROTEIN | Medicine, Experimental | Medical research | Promoters (Genetics) | Luciferase | Precocious puberty
Journal Article
Neuroendocrinology, ISSN 0028-3835, 04/2018, Volume 106, Issue 3, pp. 203 - 210
Journal Article
Arquivos Brasileiros de Endocrinologia e Metabologia, ISSN 0004-2730, 2014, Volume 58, Issue 2, pp. 108 - 117
O início da puberdade caracteriza-se pelo aumento de amplitude e frequência dos pulsos do hormônio secretor de gonadotrofinas (GnRH) após um período de... 
Gonadotropins | Genetic mutations | Gnrh analogues | Hamartomas | Central precocious puberty | ENDOCRINOLOGY & METABOLISM
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 06/2013, Volume 368, Issue 26, p. 2467
The study aims to evaluate the association, if any, between mutations in the imprinted gene MKRN3 and central precious puberty, The results indicate that a... 
Genetic aspects | Research | Gene mutations | Risk factors | Precocious puberty
Journal Article
Arquivos Brasileiros de Endocrinologia & Metabologia, ISSN 0004-2730, 03/2014, Volume 58, Issue 2, pp. 108 - 117
O início da puberdade caracteriza-se pelo aumento de amplitude e frequência dos pulsos do hormônio secretor de gonadotrofinas (GnRH) após um período de... 
Journal Article
Archives of Endocrinology and Metabolism, ISSN 2359-3997, 2016, Volume 60, Issue 6, pp. 596 - 600
Prader-Willi syndrome (PWS) is a genetic disorder frequently characterized by obesity, growth hormone deficiency, genital abnormalities, and hypogonadotropic... 
MKRN3 | MUTATIONS | GENE | DEFICIENCY | ENDOCRINOLOGY & METABOLISM | CHILDREN
Journal Article