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Human Heredity, Vol. 49, Iss. 3, 1999-05 ,pp. : 169-175

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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Identification of Non-Amplifying CYP21 Genes When Using PCR-Based Diagnosis of 21-Hydroxylase Deficiency in Congenital Adrenal Hyperplasia (CAH) Affected Pedigrees

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

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Human Molecular Genetics, Vol. 6, Iss. 4, 1997-01 ,pp. : 571-576

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CYP11B1 Mutations Causing Non-Classic Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency

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Human Molecular Genetics, Vol. 6, Iss. 11, 1997-10 ,pp. : 1829-1834

Oxford University Press

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