Lack of association between CYP21 V281L variant and polycystic ovary syndrome in Italian women.

about

Lack of association between CYP21 V281L variant and polycystic ovary syndrome in Italian women.

Item

http://www.wikidata.org/entity/Q54438820

description

2010 nî lūn-bûn

@nan

2010年の論文

@ja

2010年学术文章

@wuu

2010年学术文章

@zh

2010年学术文章

@zh-cn

2010年学术文章

@zh-hans

2010年学术文章

@zh-my

2010年学术文章

@zh-sg

2010年學術文章

@yue

2010年學術文章

@zh-hant

name

Lack of association between CY ...... ary syndrome in Italian women.

@en

Lack of association between CY ...... ary syndrome in Italian women.

@nl

type

Item

label

Lack of association between CY ...... ary syndrome in Italian women.

@en

Lack of association between CY ...... ary syndrome in Italian women.

@nl

prefLabel

Lack of association between CY ...... ary syndrome in Italian women.

@en

Lack of association between CY ...... ary syndrome in Italian women.

@nl

P1476

Lack of association between CY ...... vary syndrome in Italian women

@en

P2093

Daniela Lucchesi

http://www.w3.org/2001/XMLSchema#string

Silvia Maffei

http://www.w3.org/2001/XMLSchema#string

Stefano Del Prato

http://www.w3.org/2001/XMLSchema#string

P2860

Association of the steroid synthesis gene CYP11a with polycystic ovary syndrome and hyperandrogenism

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

A general method for isolation of high molecular weight DNA from eukaryotes

Polycystic ovary syndrome: evidence for a primary disorder of ovarian steroidogenesis.

Thirty-seven candidate genes for polycystic ovary syndrome: strongest evidence for linkage is with follistatin

The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report.

Role of the pentanucleotide (tttta)(n) polymorphism in the promoter of the CYP11a gene in the pathogenesis of hirsutism.

Novel mutations in CYP21 detected in individuals with hyperandrogenism.

Prevalence of CYP21 mutations and IRS1 variant among women with polycystic ovary syndrome and adrenal androgen excess.

Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia.

P304

596-599

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.3109/09513591003649849

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Vincenzo Longo

Laura Pucci

L Pucci

P577

2010-08-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

20201644

http://www.w3.org/2001/XMLSchema#string

P921

polycystic ovary syndrome