Associated Papers
Rare Tumor-Normal Matched Whole Exome Sequencing Identifies Novel Genomic Pathogenic Germline and Somatic Aberrations.
Sprissler R et al.
Cancers, 2020
32570879 (PubMed )
Supplement: cancers-12-01618-s001.zip › cancers-817200-Supplementary_Materials3 › Supplementary_table_S1.xlsx › Oncogenes
Association of genetic polymorphisms around the LIN28B gene and idiopathic central precocious puberty risks among Chinese girls.
Hu Z et al.
Pediatric Research, 2016
Sexual Precocity--Genetic Bases of Central Precocious Puberty and Autonomous Gonadal Activation.
Macedo DB et al.
Endocrine Development, 2016
Absence of functional LIN28B mutations in a large cohort of patients with idiopathic central precocious puberty.
Silveira-Neto AP et al.
Hormone Research in Paediatrics, 2012
New genetic factors implicated in human GnRH-dependent precocious puberty: the role of kisspeptin system.
Teles MG et al.
Molecular and Cellular Endocrinology, 2011
LIN28B, LIN28A, KISS1, and KISS1R in idiopathic central precocious puberty.
Tommiska J et al.
Bmc Research Notes, 2011
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