Analysis of the Steroidogenic Acute Regulatory Protein (StAR) Gene in Japanese Patients with Congenital Lipoid Adrenal Hyperplasia

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Oxford University Press

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Mutation Analysis in Patients with Congenital Adrenal Hyperplasia in the Spanish Population: Identification of Putative Novel Steroid 21-Hydroxylase Deficiency Alleles Associated with the Classic Form of the Disease

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Karger

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Low Frequency of CYP21B Deletions in Brazilian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

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Human Heredity, Vol. 49, Iss. 1, 1999-01 ,pp. : 9-14

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Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia

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Human Molecular Genetics, Vol. 10, Iss. 1, 2001-01 ,pp. : 39-45

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Impact of Molecular Genetics on Congenital Adrenal Hyperplasia Management

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