Phenotype-Genotype Correlations in Congenital Isolated Growth Hormone Deficiency (IGHD)
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s12098-011-0614-7.pdf
Reference57 articles.
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2. Alatzoglou KS, Dattani MT. Genetic causes and treatment of isolated growth hormone deficiency-an update. Nat Rev Endocrinol. 2010;6:562–76.
3. Alatzoglou KS, Turton JP, Kelberman D, et al. Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency. J Clin Endocrinol Metab. 2009;94:3191–9.
4. Procter AM, Phillips JA, Cooper DN. The molecular genetics of growth hormone deficiency. Hum Genet. 1998;103:255–72.
5. Wagner JK, Eble A, Hindmarsh PC, Mullis PE. Prevalence of human GH-1 gene alterations in patients with isolated growth hormone deficiency. Pediatr Res. 1998;43:105–10.
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