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Arquivos Brasileiros De Endocrinologia E Metabologia|January 6, 2012
[Clinical and molecular aspects of congenital isolated hypogonadotropic hypogonadism]Cintia Tusset, Ericka B Trarbach, Letícia Ferreira Gontijo Silveira, et al.The Journal of Clinical Endocrinology and Metabolism|July 18, 2020
Novel Genetic and Biochemical Findings of DLK1 in Children with Central Precocious Puberty: A Brazilian-Spanish StudyLuciana Montenegro, José I Labarta, Maira Piovesan, et al.European Journal of Endocrinology|September 13, 2023
Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levelsLuciana Montenegro, Carlos Seraphim, Flávia Tinano, et al.International Journal of Molecular Sciences|January 30, 2021
Low Protein Expression of both ATRX and ZNRF3 as Novel Negative Prognostic Markers of Adult Adrenocortical CarcinomaVania Balderrama Brondani, Amanda Meneses Ferreira Lacombe, Beatriz Marinho de Paula Mariani, et al.The Journal of Clinical Endocrinology and Metabolism|March 14, 2023
Novel MKRN3 Missense Mutations Associated With Central Precocious Puberty Reveal Distinct Effects on UbiquitinationJohn C Magnotto, Alessandra Mancini, Keisha Bird, et al.Cancers|March 12, 2020
High Prevalence of Alterations in DNA Mismatch Repair Genes of Lynch Syndrome in Pediatric Patients with Adrenocortical Tumors Carrying a Germline Mutation on TP53Vania Balderrama Brondani, Luciana Montenegro, Amanda Meneses Ferreira Lacombe, 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.Journal of Medical Genetics|March 11, 2020
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHDJorge Luis Granadillo, Alexander P A Stegmann, Hui Guo, et al.Pageof 1