Genetics of hypogonadotropic Hypogonadism—Human and mouse genes, inheritance, oligogenicity, and genetic counseling
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Endocrinology,Molecular Biology,Biochemistry
Reference193 articles.
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2. 'Pathogenic mosaic variants in congenital hypogonadotropic hypogonadism;Acierno;Genet. Med.,2020
3. 'New genetic findings in a large cohort of congenital hypogonadotropic hypogonadism;Amato;Eur. J. Endocrinol.,2019
4. Multipotent cell lineages in early mouse development depend on SOX2 function;Avilion;Genes Dev.,2003
5. 'Congenital hypogonadotropic hypogonadism with anosmia and gorlin features caused by a PTCH1 mutation reveals a new candidate gene for kallmann syndrome;Barraud;Neuroendocrinology,2021
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