(Q57632787)

English

Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency

scientific article published on 01 May 2000

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Influence of different genotypes on 17-hydroxyprogesterone levels in patients with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

congenital adrenal hyperplasia due to 21-hydroxylase deficiency

0 references

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Berenice Bilharinho Mendonca

6

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

A E Billerbeck

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

J A Marcondes

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

G Madureira

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

I J Arnhold

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

publication date

1 May 2000

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Clinical Endocrinology

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

52

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

601-607

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Clinical and biological phenotypes in late-onset 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00995.X

21 January 2018

Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00995.X

21 January 2018

Male pseudohermaphroditism due to nonsalt-losing 3 beta-hydroxysteroid dehydrogenase deficiency: gender role change and absence of gynecomastia at puberty

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00995.X

21 January 2018

Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00995.X

21 January 2018

Genotyping Steroid 21-Hydroxylase Deficiency: Hormonal Reference Data*

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00995.X

21 January 2018

Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00995.X

21 January 2018

Steroid 21-hydroxylase deficiency: two additional mutations in salt-wasting disease and rapid screening of disease-causing mutations.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00995.X

21 January 2018

Structure of human steroid 21-hydroxylase genes

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00995.X

21 January 2018

Identifiers

10.1046/J.1365-2265.2000.00995.X

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10792340%20AND%20SRC:MED&resulttype=core&format=json

6 November 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=Q57632787&oldid=2121304970"