Keyword "HYPOGONADOTROPIC HYPOGONADISM" found in the following publications:

A NOVEL HETEROZYGOUS VARIANT IN EXON 32 OF THE CHD7 GENE (C.6923C>T) IN A SYRIAN FAMILY WITH KALLMANN SYNDROME
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Background: Kallmann syndrome (KS) and CHARGE syndrome (CS) are rare heritable disorders in which anosmia and hypogonadotropic hypogonadism ...
Abstract | Full text (PDF)

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Research Results in Biomedicine (ISSN 2658-6533)

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The Founder: Federal State Autonomous Educational Institution of Higher Education "Belgorod National Research University"The Founder’s address: 85 Pobedy Street, Belgorod, the Belgorod region, 308015, Russia

The Publisher: Federal State Autonomous Educational Institution of HigherEducation "Belgorod National Research University" The Founder’s address:85 Pobedy Street, Belgorod, the Belgorod region, 308015, Russia

Editors Office: chief editor Mikhail I. Churnosov, e-mail: RR_MedPharm@bsu.edu.ru, phone: +7 (4722) 30-14-03.

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