Work

Variable Phenotypes in Familial Isolated Growth Hormone Deficiency Caused by a G6664A Mutation in the GH-1 Gene

Year: 2007

Type: article

Study design: Observational Study

Source: The Journal of Clinical Endocrinology & Metabolism

DOI: 10.1210/jc.2007-0684

Authors: Ora Hess, Yasir Hujeirat, Michael P. Wajnrajch, Stavit Allon-Shalev, Zvi Zadik, Idit Lavi, Yardena Tenenbaum-Rakover

Institutions: Bar-Ilan University, Emek Medical Center, Pfizer (United States), Technion – Israel Institute of Technology, Hebrew University of Jerusalem, Kaplan Medical Center, Carmel Medical Center

Language: English

Topic: Growth Hormone and Insulin-like Growth Factors

Subfield: Endocrinology, Diabetes and Metabolism

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2045732936

FWCI: 1.712

Cites: 28

Cited by: 33

Related to: 10