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Exome Sequencing as a Tool for Detecting Point Mutations and Deletions in Patients With Hypogonadotropic Hypogonadism

Jacques Young1

  • 1Université Paris-Saclay, Assistance Publique-Hôpitaux de Paris, Department of Reproductive Endocrinology and INSERM U1185, Bicêtre Hospital, F-94275, Le Kremlin-Bicêtre, France.

The Journal of Clinical Endocrinology and Metabolism
|June 21, 2022
PubMed
Abstract

No abstract available in PubMed .

Keywords:
GnRHKallmann syndromecongenital hypogonadotropic hypogonadismdelayed pubertyexomegonadotropin deficiency

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