Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency (Q69891525)

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scientific article published on 01 December 1986

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Language	Label	Description	Also known as
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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instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

title

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

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

author

Jean Dausset

series ordinal

8

object named as

J Dausset

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

author name string

E Mornet

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

P Couillin

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

F Kutten

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

M C Raux

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

P C White

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

D Cohen

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

A Boué

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

publication date

1 December 1986

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

volume

74

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

page(s)

402-408

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

cites work

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

1 reference

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

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/2878869

retrieved

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

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human C4 haplotypes with duplicated C4A or C4B

1 reference

stated in

PubMed

reference URL

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

retrieved

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

stated in

PubMed

reference URL

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

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00280494

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

Dimensions Publication ID

1003583788

0 references

PubMed publication ID

2878869

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2878869

reference URL

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

retrieved

6 October 2019

 

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