(Q28307538)

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Mayer-Rokitansky-Kuster-Hauser syndrome: recent clinical and genetic findings

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Europe PubMed Central

title

Mayer-Rokitansky-Kuster-Hauser syndrome: recent clinical and genetic findings (English)

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Pascal Philibert

3

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author name string

Charles Sultan

series ordinal

1

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Anna Biason-Lauber

series ordinal

2

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language of work or name

English

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publication date

January 2009

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published in

Gynecological Endocrinology

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volume

25

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issue

1

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page(s)

8-11

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cites work

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080/09513590802288291

retrieved

21 April 2017

Clinical aspects of Mayer-Rokitansky-Kuester-Hauser syndrome: recommendations for clinical diagnosis and staging

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F09513590802288291

retrieved

21 January 2018

DNA sequence variations of the entire anti-Mullerian hormone (AMH) gene promoter and AMH protein expression in patients with the Mayer-Rokitanski-Kuster-Hauser syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F09513590802288291

retrieved

21 January 2018

Further evidence that the WT1 gene does not have a role in the development of the derivatives of the müllerian duct.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F09513590802288291

retrieved

21 January 2018

The N314D polymorphism of the GALT gene is not associated with congenital absence of the uterus and vagina

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F09513590802288291

retrieved

21 January 2018

Analysis of cystic fibrosis transmembrane conductance regulator gene mutations in patients with congenital absence of the uterus and vagina.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F09513590802288291

retrieved

21 January 2018

The role of HOX genes in human implantation

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F09513590802288291

retrieved

21 January 2018

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F09513590802288291

retrieved

21 January 2018

A novel syndrome of diabetes mellitus, renal dysfunction and genital malformation associated with a partial deletion of the pseudo-POU domain of hepatocyte nuclear factor-1beta

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F09513590802288291

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F09513590802288291

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F09513590802288291

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1080%2F09513590802288291

retrieved

21 January 2018

Identifiers

DOI

10.1080/09513590802288291

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4131900

OpenCitations bibliographic resource ID

4131900

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4131900

PubMed publication ID

19165657

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4131900

(Q28307538)

Mayer-Rokitansky-Kuster-Hauser syndrome: recent clinical and genetic findings

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