(Q33694897)

28 July 2017

1 reference

title

Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment (English)

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congenital adrenal hyperplasia

28 July 2017

0 references

1 reference

A D Carlson

1

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28 July 2017

J S Obeid

2

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28 July 2017

N Kanellopoulou

3

1 reference

28 July 2017

R C Wilson

4

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28 July 2017

M I New

5

1 reference

28 July 2017

publication date

1 April 1999

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The Journal of Steroid Biochemistry and Molecular Biology

28 July 2017

published in

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28 July 2017

volume

69

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28 July 2017

issue

1-6

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28 July 2017

page(s)

19-29

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Newborn screening, prenatal diagnosis, and prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

28 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

Structure of human steroid 21-hydroxylase genes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

Effects of individual mutations in the P-450(C21) pseudogene on the P-450(C21) activity and their distribution in the patient genomes of congenital steroid 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

Aberrant splicing and missense mutations cause steroid 21-hydroxylase [P-450(C21)] deficiency in humans: possible gene conversion products

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

Prenatal diagnosis and treatment of 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-0760%2899%2900059-X

7 January 2021

10.1016/S0960-0760(99)00059-X

Identifiers

DOI

1 reference

28 July 2017

1 reference