Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia

Authors:	Rainbow L A Rees S A Shaikh M G Shaw N J Cole T Barrett T G Kirk J M W

Affiliation:	Department of Medical and Molecular Genetics, University of Birmingham, Birmingham, UK.

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