Open AccessReproductive Phenotypes and Genotypes in Men With IHH
Author(s) -
Andrew A. Dwyer,
Maria Stamou,
Ella Anghel,
Shira Hornstein,
DanNa Chen,
Kathryn Salnikov,
Isabella R McDonald,
Lacey Plummer,
Stephanie B. Seminara,
Ravikumar Balasubramanian
Publication year - 2022
Publication title -
the journal of clinical endocrinology and metabolism/journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/clinem/dgac615
Subject(s) - kallmann syndrome , medicine , endocrinology , hypogonadotropic hypogonadism , luteinizing hormone , gnrhr , biology , genotype , delayed puberty , hormone , gonadotropin releasing hormone , gene , genetics , disease , covid-19 , infectious disease (medical specialty)
Isolated hypogonadotropic hypogonadism (IHH) is phenotypically and genetically heterogeneous.