(Q39911408)

15 September 2017

Premature pubarche in Mediterranean girls: high prevalence of heterozygous CYP21 mutation carriers (English)

1 reference

15 September 2017

1 reference

Françoise Paris

1

1 reference

15 September 2017

Véronique Tardy

2

1 reference

15 September 2017

Anne Chalançon

3

1 reference

15 September 2017

Marie Christine Picot

4

1 reference

15 September 2017

Yves Morel

5

1 reference

15 September 2017

Charles Sultan

6

1 reference

15 September 2017

1 May 2010

1 reference

Gynecological Endocrinology

15 September 2017

1 reference

15 September 2017

26

1 reference

15 September 2017

319-324

1 reference

15 September 2017

5

1 reference

Developmental changes in steroidogenic enzymes in human postnatal adrenal cortex: immunohistochemical studies.

15 September 2017

1 reference

https://api.crossref.org/works/10.3109%2F09513590903511505

Serine phosphorylation of human P450c17 increases 17,20-lyase activity: implications for adrenarche and the polycystic ovary syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903511505

Adrenarche - physiology, biochemistry and human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903511505

'Exaggerated adrenarche' in children presenting with premature adrenarche

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903511505

Molecular defects of the CYP21 gene in Spanish girls with isolated precocious pubarche.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903511505

Candidate gene analysis in premature pubarche and adolescent hyperandrogenism

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903511505

Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903511505

Extensive clinical experience: nonclassical 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903511505

p.H62L, a rare mutation of the CYP21 gene identified in two forms of 21-hydroxylase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903511505

Early onset of puberty: tracking genetic and environmental factors

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903511505

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/10.3109%2F09513590903511505

Genetic defects of steroidogenesis in premature pubarche

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903511505

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/10.3109%2F09513590903511505

Novel mutations in CYP21 detected in individuals with hyperandrogenism.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F09513590903511505

10.3109/09513590903511505

21 January 2018

Identifiers

DOI

1 reference

15 September 2017

1 reference