First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination (Q70146141)

From Wikidata

Jump to navigation Jump to search

scientific article published on 01 August 1986

Language	Label	Description	Also known as
English	First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination	scientific article published on 01 August 1986

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

7

object named as

J Dausset

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

author name string

E Mornet

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

J Boue

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

M Raux-Demay

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

P Couillin

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

J F Oury

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

Y Dumez

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

D Cohen

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

A Boué

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

publication date

1 August 1986

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

73

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

358-364

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

https://scigraph.springernature.com/pub.10.1007/bf00279101

0 references

HLA typing of amniotic-fluid cells applied to prenatal diagnosis of congenital adrenal hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA polymorphism of HLA class I and class II regions

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA associations in 21-hydroxylase deficiency (congenital and late-onset adrenal hyperplasia) in France

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clusters of HLA class II beta restriction fragments describe allelic series

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and partial nucleotide sequence of a cDNA clone for human histocompatibility antigen HLA-B by use of an oligodeoxynucleotide primer

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations and selection in the generation of class II histocompatibility antigen polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

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/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal Diagnosis of Sickle-Cell Anemia in the First Trimester of Pregnancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotyping with DNA probes in combined immunodeficiency syndrome with defective expression of HLA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

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/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency by steroid analysis in the amniotic fluid of mid-pregnancy: comparison with HLA typing in 17 pregnancies at risk for CAH

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of HLA class I genes with restriction endonuclease fragments: implications for polymorphism of the human major histocompatibility complex

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The biochemical basis for genotyping 21-hydroxylase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

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/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct gene analysis of chorionic villi: A possible technique for first-trimester antenatal diagnosis of haemoglobinopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA and congenital adrenal hyperplasia linkage confirmed

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3017844

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/3017844

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/3017844

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00279101

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3017844%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q70146141&oldid=2143965657"