Mullerian dysgenesis: a critical review of the literature.

about

Porous poly-l-lactide-co-ɛ-caprolactone scaffold: a novel biomaterial for vaginal tissue engineering

P2860

Q58776297-DFCA234E-073A-4950-8E4A-000CFA6FB015

P2860

Mullerian dysgenesis: a critical review of the literature.

Item

http://www.wikidata.org/entity/Q39256834

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Mullerian dysgenesis: a critical review of the literature.

@en

Mullerian dysgenesis: a critical review of the literature.

@nl

type

Item

label

Mullerian dysgenesis: a critical review of the literature.

@en

Mullerian dysgenesis: a critical review of the literature.

@nl

prefLabel

Mullerian dysgenesis: a critical review of the literature.

@en

Mullerian dysgenesis: a critical review of the literature.

@nl

P1476

Mullerian dysgenesis: a critical review of the literature.

@en

P2093

Dimitrios Nasioudis

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

Dimitrios Schizas

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

Souzana Choussein

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

P2860

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).

A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman

WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report

Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study

The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches

Sexually dimorphic sterility phenotypes in Hoxa10-deficient mice

Hox10 and Hox11 genes are required to globally pattern the mammalian skeleton

WNT7A mutations in patients with Müllerian duct abnormalities

Wnt5a is required for proper epithelial-mesenchymal interactions in the uterus

P2888

s00404-017-4372-2

P304

1369-1381

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

P31

scholarly article

P356

10.1007/S00404-017-4372-2

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

P433

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

P478

295

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

P50

Konstantinos P. Economopoulos

P577

2017-04-22T00:00:00Z

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

P698

28434104

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

Mullerian dysgenesis: a critical review of the literature.

about

P2860

P2860

Mullerian dysgenesis: a critical review of the literature.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698