Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and GNRH1[original query] |
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Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1. Clinical endocrinology 2010 Mar 72 (3): 371-6. Trarbach Ericka Barbosa, Teles Milena Gurgel, Costa Elaine Maria Frade, Abreu Ana Paula, Garmes Heraldo Mendes, Guerra Gil, Baptista Maria Tereza Matias, de Castro Margaret, Mendonca Berenice Bilharinho, Latronico Ana Claud |
Identification of selected genetic polymorphisms in polycystic ovary syndrome in Sri Lankan women using low cost genotyping techniques. PloS one 2019 1 13 (12): e0209830. Branavan Umayal, Muneeswaran Kajan, Wijesundera Sulochana, Jayakody Surangi, Chandrasekharan Vishvanath, Wijeyaratne Chandri |
The functional study of a novel MKRN3 missense mutation associated with familial central precocious puberty. American journal of medical genetics. Part A 2023 12 . Ziwei Chen, Qing You, Junqi Wang, Zhiya Dong, Wei Wang, Yuanyan Yang, Xiaoyu Ma, Chuanyin Li, Wenli |
Genetic Variants of Steroidogenesis and Gonadotropin Pathways and Polycystic Ovary Syndrome Susceptibility: A Systematic Review and Meta-analysis. Metabolic syndrome and related disorders 2023 10 . Priya Sharma, Abhilash Kumar Singh, Sabyasachi Senapati, Harmanpreet Singh Kapoor, Lajya Devi Goyal, Balpreet Kaur, Pooja Kamra, Preeti Khetarp |
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