(Q83377310)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712666%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

title

Hyperandrogenism in carriers of CYP21 mutations: the role of genotype (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712666%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference

Osnat Admoni

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712666%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Shosh Israel

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712666%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Idit Lavi

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712666%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Michal Gur

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712666%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Yardena Tenenbaum-Rakover

5

1 reference

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21 January 2020

publication date

1 June 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712666%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

published in

Clinical Endocrinology

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712666%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

volume

64

1 reference

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21 January 2020

issue

6

1 reference

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21 January 2020

page(s)

645-651

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712666%20AND%20SRC:MED&resulttype=core&format=json

Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

21 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Congenital adrenal hyperplasias

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Congenital adrenal hyperplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Screening for 21-hydroxylase-deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Identification of heterozygotic carriers of 21-hydroxylase deficiency: sensitivity of ACTH stimulation tests

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Molecular abnormalities of the 21-hydroxylase gene in hyperandrogenic women with an exaggerated 17-hydroxyprogesterone response to short-term adrenal stimulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Exhaustive screening of the 21-hydroxylase gene in a population of hyperandrogenic women

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Hyperandrogenism and manifesting heterozygotes for 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Exaggerated 17-hydroxyprogesterone response to short-term adrenal stimulation and evidence for CYP21B gene point mutations in true precocious puberty

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Carriers of 21-hydroxylase deficiency are not at increased risk for hyperandrogenism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

The presence of the 21-hydroxylase deficiency carrier status in hirsute women: phenotype-genotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Phenotype-Genotype Correlation in 56 Women with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Steroid 21-hydroxylase (P450c21): a new allele and spread of mutations through the pseudogene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Variable ACTH-stimulated 17-hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

Structural and functional analysis of a novel mutation of CYP21B in a heterozygote carrier of 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02521.X

10.1111/J.1365-2265.2006.02521.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16712666%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference