(Q34246234)

31 July 2017

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title

Prenatal treatment of congenital adrenal hyperplasia. The United States experience (English)

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31 July 2017

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M I New

1

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31 July 2017

publication date

1 March 2001

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Endocrinology and Metabolism Clinics of North America

31 July 2017

published in

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31 July 2017

volume

30

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31 July 2017

issue

1

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31 July 2017

page(s)

1-13

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Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency

31 July 2017

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The structural basis of the multiple forms of human complement component C4.

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Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment

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Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.

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Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8

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7 January 2021

Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency).

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7 January 2021

Prenatal treatment in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: up-date 88 of the French multicentric study

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7 January 2021

Prenatal diagnosis and treatment of 21-hydroxylase deficiency

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Nonsense mutation causing steroid 21-hydroxylase deficiency

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Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene

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The human gene mutation database

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Long-term somatic follow-up of prenatally treated children with congenital adrenal hyperplasia.

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Novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11 beta-hydroxylase deficiency.

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The P450 superfamily: update on new sequences, gene mapping, and recommended nomenclature

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Genotyping Steroid 21-Hydroxylase Deficiency: Hormonal Reference Data*

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Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Newborn screening and its relationship to the diagnosis and treatment of the disorder

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High frequency of congenital adrenal hyperplasia (classic 11 beta-hydroxylase deficiency) among Jews from Morocco

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7 January 2021

How safe is long-term prenatal glucocorticoid treatment?

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7 January 2021

Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1

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7 January 2021

Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms

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7 January 2021

A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele

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7 January 2021

A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin

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7 January 2021

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man

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7 January 2021

Structure of human steroid 21-hydroxylase genes

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7 January 2021

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

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7 January 2021

Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene

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7 January 2021

Clinical and biochemical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. A study of 25 patients

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7 January 2021

Prevalence of nonclassical steroid 21-hydroxylase deficiency based on a morning salivary 17-hydroxyprogesterone screening test: a small sample study

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7 January 2021

10.1016/S0889-8529(08)70016-1

Identifiers

DOI

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31 July 2017

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