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Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

Endocrinology and metabolism clinics of North America, 2001-03, Vol.30 (1), p.31

Speiser, P W

2001

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21-Hydroxylase–deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study

American journal of obstetrics and gynecology, 2000-12, Vol.183 (6), p.1468-1474

2000

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An update on the frequency of nonclassic deficiency of adrenal 21-hydroxylase in the Yugoslav population

Acta endocrinologica (Copenhagen), 1990-06, Vol.122 (6), p.703

1990

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Genotyping of CYP21, linked chromosome 6p markers, and a sex-specific gene in neonatal screening for congenital adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 1999-03, Vol.84 (3), p.960-966

1999

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Genotype and hormonal phenotype in nonclassical 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1987, Vol.64 (1), p.86-91

1987

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Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Socie Clinical Practice Guideline

The journal of clinical endocrinology and metabolism, 2010, Vol.95 (9), p.4133-4160

2010

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Mutations in the CYP11B1 Gene Causing Congenital Adrenal Hyperplasia and Hypertension Cluster in Exons 6, 7, and 8

Proceedings of the National Academy of Sciences - PNAS, 1993-05, Vol.90 (10), p.4552-4556

1993

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Detection of Steroid 21-Hydroxylase Alleles Using Gene-Specific PCR and a Multiplexed Ligation Detection Reaction

Genomics (San Diego, Calif.), 1995-09, Vol.29 (1), p.152-162

1995

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Insulin insensitivity in adrenal hyperplasia due to nonclassical steroid 21-hydroxylase deficiency

The journal of clinical endocrinology and metabolism, 1992-12, Vol.75 (6), p.1421-1424

1992

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Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

Clinical endocrinology (Oxford), 1998-10, Vol.49 (4), p.411-417

1998

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Study of a kindred with classic congenital adrenal hyperplasia : Diagnostic challenge due to phenotypic variance

The journal of clinical endocrinology and metabolism, 1998-06, Vol.83 (6), p.1940-1945

1998

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Steroid 11 beta-hydroxylase deficiency and related disorders

Endocrinology and metabolism clinics of North America, 1994-06, Vol.23 (2), p.325

1994

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Genetics of adrenal steroid 21-hydroxylase deficiency

Endocrine reviews, 1986-08, Vol.7 (3), p.331-349

1986

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Splicing mutation in CYP21 associated with delayed presentation of salt-wasting congenital adrenal hyperplasia

American journal of medical genetics, 1995-07, Vol.57 (3), p.450-454

1995

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Excess mineralocorticoid receptor activity in patients with dexamethasone-suppressible hyperaldosteronism is under adrenocorticotropin control

The journal of clinical endocrinology and metabolism, 1985-08, Vol.61 (2), p.297-302

1985

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Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Human genetics, 1992-03, Vol.88 (6), p.647-648

1992

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Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

21-Hydroxylase–deficient nonclassic adrenal hyperplasia is a progressive disorder: A multicenter study

An update on the frequency of nonclassic deficiency of adrenal 21-hydroxylase in the Yugoslav population

Genotyping of CYP21, linked chromosome 6p markers, and a sex-specific gene in neonatal screening for congenital adrenal hyperplasia

Genotype and hormonal phenotype in nonclassical 21-hydroxylase deficiency

Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Socie Clinical Practice Guideline

Mutations in the CYP11B1 Gene Causing Congenital Adrenal Hyperplasia and Hypertension Cluster in Exons 6, 7, and 8

Detection of Steroid 21-Hydroxylase Alleles Using Gene-Specific PCR and a Multiplexed Ligation Detection Reaction

Insulin insensitivity in adrenal hyperplasia due to nonclassical steroid 21-hydroxylase deficiency

Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

Study of a kindred with classic congenital adrenal hyperplasia : Diagnostic challenge due to phenotypic variance

Steroid 11 beta-hydroxylase deficiency and related disorders

Genetics of adrenal steroid 21-hydroxylase deficiency

Splicing mutation in CYP21 associated with delayed presentation of salt-wasting congenital adrenal hyperplasia

Excess mineralocorticoid receptor activity in patients with dexamethasone-suppressible hyperaldosteronism is under adrenocorticotropin control

Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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