High frequency of nonclassical steroid 21-hydroxylase deficiency (Q34465309)

2 August 2017

title

High frequency of nonclassical steroid 21-hydroxylase deficiency (English)

1 reference

2 August 2017

P W Speiser

1

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2 August 2017

B Dupont

2

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2 August 2017

P Rubinstein

3

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2 August 2017

A Piazza

4

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2 August 2017

A Kastelan

5

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2 August 2017

M I New

6

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2 August 2017

language of work or name

English

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publication date

1 July 1985

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American Journal of Human Genetics

2 August 2017

published in

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2 August 2017

volume

37

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2 August 2017

issue

4

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2 August 2017

page(s)

650-667

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Virilizing adrenal hyperplasia; a genetic and hormonal study

2 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684620

HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684620

Neonatal screening for congenital adrenal hyperplasia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684620

Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684620

Recent Advances in 21-Hydroxylase Deficiency

6 July 2018

1 reference

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HLA and Disease 1982 - A Survey

6 July 2018

1 reference

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HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation

6 July 2018

1 reference

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Genotyping Steroid 21-Hydroxylase Deficiency: Hormonal Reference Data*

6 July 2018

1 reference

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The Attenuated Form of Congenital Adrenal Hyperplasia as an Allelic Form of 21-Hydroxylase Deficiency*

6 July 2018

1 reference

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Linkage of Chido and HL-A.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684620

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684620

Rga (Rodgers) and the HLA region: linkage and associations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684620

Gene frequencies and genetic linkage disequilibrium for the HLA-linked genes Bf, C2, C4S, C4F, 21-hydroxylase deficiency, and glyoxalase I

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684620

Possible genetic linkage disequilibrium between HLA and the 21-hydroxylase deficiency gene (congenital adrenal hyperplasia)

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684620

Hormonal Phenotype and HLA-Genotype in Families of Patients with Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency)

6 July 2018

1 reference

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Mineralocorticoids, salt balance and blood pressure after prolonged ACTH administration in juvenile hypertension

6 July 2018

1 reference

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Serum Androgens as a Continuing Index of Adequacy of Treatment of Congenital Adrenal Hyperplasia*

6 July 2018

1 reference

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Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typing

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684620

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684620

HLA polymorphism in Israel. 9. An overall comparative analysis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684620

Mapping of the 21-hydroxylase deficiency gene within the HLA linkage group

27 October 2018

1 reference

12 December 2020

The use of cortisone in follicular phase disturbances

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12 December 2020

Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia

1 reference

12 December 2020

Adult-onset familial adrenal 21-hydroxylase deficiency

1 reference

12 December 2020

Late-Onset Steroid 21-Hydroxylase Deficiency: A Variant of Classical Congenital Adrenal Hyperplasia*

1 reference

12 December 2020

Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency

1 reference

12 December 2020

Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: A new Allele at the 21-hydroxylase locus

1 reference

12 December 2020

Studies of the C-21 and C-19 Steroids and HLA Genotyping in Siblings and Parents of Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency*

1 reference

12 December 2020

HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency

1 reference

12 December 2020

Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group

1 reference

12 December 2020

[Clinically late virilism with excretion of pregnanetriol and insufficiency of cortisol production]

1 reference

12 December 2020

Chido and Rodgers blood groups: relationship to C4 and HLA

1 reference

12 December 2020

Microdroplet Assay of Human Serum Cytotoxins

1 reference

12 December 2020

Identifiers

PMC publication ID

1684620

1 reference

2 August 2017

1 reference