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Showing results (131-140 of 137) with videos related to

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Hormone Research in Paediatrics|September 12, 2012
Absence of functional LIN28B mutations in a large cohort of patients with idiopathic central precocious pubertyAcácio P Silveira-Neto, Leticia Ferro Leal, Amy B Emerman, et al.
The New England Journal of Medicine|June 7, 2013
Central precocious puberty caused by mutations in the imprinted gene MKRN3Ana Paula Abreu, Andrew Dauber, Delanie B Macedo, et al.
The Journal of Infectious Diseases|September 16, 2011
TNF -308G>A single nucleotide polymorphism is associated with leprosy among Brazilians: a genetic epidemiology assessment, meta-analysis, and functional studyCynthia C Cardoso, Ana Carla Pereira, Vânia N Brito-de-Souza, et al.
The Journal of Infectious Diseases|April 3, 2013
Toll-like receptor 1 N248S single-nucleotide polymorphism is associated with leprosy risk and regulates immune activation during mycobacterial infectionCarolinne de Sales Marques, Vânia N Brito-de-Souza, Luana Tatiana Albuquerque Guerreiro, et al.
The Journal of Clinical Endocrinology and Metabolism|March 18, 2014
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3Delanie B Macedo, Ana Paula Abreu, Ana Claudia S Reis, et al.
The Journal of Clinical Endocrinology and Metabolism|December 31, 2020
Genotype-Phenotype Correlations in Central Precocious Puberty Caused by MKRN3 MutationsCarlos Eduardo Seraphim, Ana Pinheiro Machado Canton, Luciana Montenegro, et al.
The Lancet. Diabetes & Endocrinology|June 29, 2023
Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort studyAna P M Canton, Flávia R Tinano, Leonardo Guasti, et al.
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Showing results (131-140 of 137) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 137 results.
Hormone Research in Paediatrics|September 12, 2012
Absence of functional LIN28B mutations in a large cohort of patients with idiopathic central precocious pubertyAcácio P Silveira-Neto, Leticia Ferro Leal, Amy B Emerman, et al.
The New England Journal of Medicine|June 7, 2013
Central precocious puberty caused by mutations in the imprinted gene MKRN3Ana Paula Abreu, Andrew Dauber, Delanie B Macedo, et al.
The Journal of Infectious Diseases|September 16, 2011
TNF -308G>A single nucleotide polymorphism is associated with leprosy among Brazilians: a genetic epidemiology assessment, meta-analysis, and functional studyCynthia C Cardoso, Ana Carla Pereira, Vânia N Brito-de-Souza, et al.
The Journal of Infectious Diseases|April 3, 2013
Toll-like receptor 1 N248S single-nucleotide polymorphism is associated with leprosy risk and regulates immune activation during mycobacterial infectionCarolinne de Sales Marques, Vânia N Brito-de-Souza, Luana Tatiana Albuquerque Guerreiro, et al.
The Journal of Clinical Endocrinology and Metabolism|March 18, 2014
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3Delanie B Macedo, Ana Paula Abreu, Ana Claudia S Reis, et al.
The Journal of Clinical Endocrinology and Metabolism|December 31, 2020
Genotype-Phenotype Correlations in Central Precocious Puberty Caused by MKRN3 MutationsCarlos Eduardo Seraphim, Ana Pinheiro Machado Canton, Luciana Montenegro, et al.
The Lancet. Diabetes & Endocrinology|June 29, 2023
Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort studyAna P M Canton, Flávia R Tinano, Leonardo Guasti, et al.
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