A molecular basis for variation in clinical severity of isolated growth hormone deficiency type II.

Hamid R, Phillips JA, Holladay C, Cogan JD, Austin ED, Backeljauw PF, Travers SH, Patton JG
J Clin Endocrinol Metab. 2009 94 (12): 4728-34

PMID: 19837935 · PMCID: PMC2795644 · DOI:10.1210/jc.2009-0746

MeSH Terms (16)

Alleles Cell Line DNA Dwarfism, Pituitary Exons Female Genetic Markers Genetic Variation Genotype Human Growth Hormone Humans Male Mutation Pedigree Pituitary Gland Transcription, Genetic

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