(Q69891525)

English

Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency

scientific article published on 01 December 1986

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878869%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878869%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

8

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J Dausset

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Europe PubMed Central

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6 October 2019

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E Mornet

1

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6 October 2019

P Couillin

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878869%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

F Kutten

3

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6 October 2019

M C Raux

4

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6 October 2019

P C White

5

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6 October 2019

D Cohen

6

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6 October 2019

A Boué

7

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6 October 2019

publication date

1 December 1986

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6 October 2019

1 reference

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6 October 2019

74

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6 October 2019

4

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6 October 2019

402-408

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6 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00280494

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878869

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878869

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphic restriction endonuclease fragment segregates and correlates with the gene for HLA-B8

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878869

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA and 21 hydroxylase deficiency (congenital and late onset adrenal hyperplasia) in the French population

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878869

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878869

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878869

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878869

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning and expression of cDNA encoding a bovine adrenal cytochrome P-450 specific for steroid 21-hydroxylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878869

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878869

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878869

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human C4 haplotypes with duplicated C4A or C4B

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878869

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878869

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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