Variable phenotypes in familial isolated growth hormone deficiency caused by a G6664A mutation in the GH-1 gene.

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

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

Affiliation

Hess O; Faculty of Sciences, Bar Ilan University, Ramat Gan 52900, Israel.

J Clin Endocrinol Metab ; 92(11): 4387-93, 2007 Nov.

Article in En | MEDLINE | ID: mdl-17785368

Subject(s)

Human Growth Hormone/deficiency; Human Growth Hormone/genetics; Mutation/genetics; Mutation/physiology; Adolescent; Adult; Aged; Aged, 80 and over; Arabs; Child; Child, Preschool; DNA/genetics; DNA Mutational Analysis; Female; Genotype; Human Growth Hormone/blood; Humans; Infant; Insulin-Like Growth Factor I/metabolism; Jews; Male; Middle Aged; Pedigree; Phenotype; Twins

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Database: MEDLINE Main subject: Human Growth Hormone / Mutation Type of study: Guideline Limits: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: J Clin Endocrinol Metab Year: 2007 Type: Article Affiliation country: Israel

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