The association of +1150A polymorphism with low GH level in isolated growth hormone deficiency (IGHD) patients

Author:

Esmaiel Nora N.ORCID,Fayez Alaaeldin G.ORCID,Thomas Manal M.,Khalaf Randa I.,Salem Sohair M.,Ramadan Abeer,Helwa Iman,Raouf Haiam Abdel,El-Bassyouni Hala T.ORCID,Ismaeil Samira

Publisher

Elsevier BV

Subject

Genetics

Reference28 articles.

1. Association between fetal growth restriction and polymorphisms at sites −1 and +3 of pituitary growth hormone: a case-control study;Adkins;BMC Pregnancy Childbirth,2005

2. Genetic causes and treatment of isolated growth hormone deficiency-an update;Alatzoglou;Nat. Rev. Endocrinol.,2010

3. HALCyon study team. A multi-cohort study of polymorphisms in the GH/IGF axis and physical capability: the HALCyon programme;Alfred;PLoS One,2012

4. Genetic characterization of growth hormone 1 gene in patients with isolated growth hormone deficiency;Birla;Ind. J. Endocrinol. Metab.,2012

5. Genetic defects in GH synthesis and secretion;Bona;Eur. J. Endocrinol.,2004

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