Familial Leydig Cell Hypoplasia as a Cause of Male Pseudohermaphroditism
Author:
Publisher
S. Karger AG
Subject
Genetics (clinical),Genetics
Cited by 33 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Restoring function to inactivating G protein‐coupled receptor variants in the hypothalamic–pituitary–gonadal axis1;Journal of Neuroendocrinology;2024-06-09
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3. Receptor Transduction Pathways Mediating Hormone Action;Sperling Pediatric Endocrinology;2021
4. Novel mutations of the LHCGR gene in two families with 46,XY DSD causing Leydig cell hypoplasia I;Hormones;2020-07-14
5. Loss-of-Function Mutations in the Human Luteinizing Hormone Receptor Predominantly Cause Intracellular Retention;Endocrinology;2016-08-17
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