Frequent deletion and duplication of the steroid 21-hydroxylase genes (Q35198772)

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English	Frequent deletion and duplication of the steroid 21-hydroxylase genes	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3490178

retrieved

7 August 2017

title

Frequent deletion and duplication of the steroid 21-hydroxylase genes (English)

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stated in

Europe PubMed Central

PubMed publication ID

3490178

retrieved

7 August 2017

author name string

J W Werkmeister

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3490178

retrieved

7 August 2017

M I New

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3490178

retrieved

7 August 2017

B Dupont

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3490178

retrieved

7 August 2017

P C White

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3490178

retrieved

7 August 2017

language of work or name

English

0 references

publication date

1 October 1986

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3490178

retrieved

7 August 2017

published in

American Journal of Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3490178

retrieved

7 August 2017

volume

39

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3490178

retrieved

7 August 2017

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3490178

retrieved

7 August 2017

page(s)

461-469

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3490178

retrieved

7 August 2017

cites work

High frequency of nonclassical steroid 21-hydroxylase deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

A highly polymorphic locus in human DNA

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

Human C4 haplotypes with duplicated C4A or C4B

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

Detection of sickle cell beta S-globin allele by hybridization with synthetic oligonucleotides

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

Structure and organization of theC4genes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

Structure of human steroid 21-hydroxylase genes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

Restriction maps and restriction fragment length polymorphisms of the human 21-hydroxylase genes.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

Inborn errors of steroid biosynthesis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683994

retrieved

28 July 2018

The biochemical basis for genotyping 21-hydroxylase deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3490178

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3490178

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extended MHC haplotypes in 21-hydroxylase-deficiency congenital adrenal hyperplasia: shared genotypes in unrelated patients

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3490178

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rearrangement of 21-hydroxylase genes in disease-associated MHC supratypes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3490178

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is salt-wasting in congenital adrenal hyperplasia due to the same gene as the fasciculata defect?

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3490178

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1683994

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3490178

retrieved

7 August 2017

PubMed publication ID

3490178

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3490178

retrieved

7 August 2017

 

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