(Q25255341)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16441882%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

review article

2 references

6 February 2021

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16441882%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

0 references

3 references

13 March 2019

9 October 2019

6 February 2021

1 reference

9 October 2019

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16441882%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

author name string

Thomas Mouchel

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16441882%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Laurent Pasquier

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16441882%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Isabelle Pellerin

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16441882%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

language of work or name

English

0 references

publication date

27 January 2006

4 references

13 March 2019

9 October 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16441882%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

6 February 2021

Journal of Negative Results in BioMedicine

3 references

9 October 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16441882%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

6 February 2021

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16441882%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

issue

1

0 references

page(s)

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16441882%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 2.0 Generic

16 January 2020

copyright license

3 references

13 March 2019

9 October 2019

on focus list of Wikimedia project

6 February 2021

copyright status

copyrighted

0 references

ScienceSource

0 references

cites work

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7 April 2017

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

7 April 2017

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

7 April 2017

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Requirement of Bmpr1a for Müllerian duct regression during male sexual development

7 April 2017

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A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome

7 April 2017

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Female development in mammals is regulated by Wnt-4 signalling

7 April 2017

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Wnt signaling in oncogenesis and embryogenesis--a look outside the nucleus

7 April 2017

1 reference

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Developmental genetics of the female reproductive tract in mammals

7 April 2017

1 reference

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Congenital abnormalities of body patterning: embryology revisited

28 September 2017

1 reference

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Congenital malformations of the genital tract and their management

28 September 2017

1 reference

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Hox genes and kidney patterning

28 September 2017

1 reference

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Disorders of androgen action

28 September 2017

1 reference

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Solitary functioning kidney and diverse genital tract malformations associated with hepatocyte nuclear factor-1beta mutations

28 September 2017

1 reference

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VATER non-random association of congenital malformations: study based on data from four malformation registers

28 September 2017

1 reference

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Müllerian agenesis: etiology, diagnosis, and management

28 September 2017

1 reference

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Genetics of the female reproductive ducts

28 September 2017

1 reference

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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

28 September 2017

1 reference

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Fetal exposure to DES results in de-regulation of Wnt7a during uterine morphogenesis

28 September 2017

1 reference

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MURCS association: case report and review

28 September 2017

1 reference

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Anti-müllerian hormone: the Jost factor.

28 September 2017

1 reference

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Mayer-Rokitansky-Kuster-Hauser syndrome with immature teratoma of the ovary at age 4 years

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

28 September 2017

1 reference

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Renal--skeletal--ear- and facial-anomalies in combination with the Mayer--Rokitansky--Küster (MRK) syndrome

28 September 2017

1 reference

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The VATER association. Vertebral defects, Anal atresia, T-E fistula with esophageal atresia, Radial and Renal dysplasia: a spectrum of associated defects

28 September 2017

1 reference

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28 September 2017

1 reference

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Congenital anomalies of the müllerian system

28 September 2017

1 reference

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Rokitansky sequence in association with the facio-auriculo-vertebral sequence: part of a mesodermal malformation spectrum?

28 September 2017

1 reference

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Congenital absence of the vagina. The Mayer-Rokitansky-Kuster-Hauser syndrome

28 September 2017

1 reference

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The MURCS association: Müllerian duct aplasia, renal aplasia, and cervicothoracic somite dysplasia

28 September 2017

1 reference

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A preliminary report on gonadotropin responsivity in the Rokitansky-Küster-Hauser syndrome (congenitally absent uterus)

28 September 2017

1 reference

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Relationship between Mayer-Rokitansky-Küster (MRK) anomaly and hereditary renal adysplasia (HRA)

28 September 2017

1 reference

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Differential expression patterns of Wnt genes in the murine female reproductive tract during development and the estrous cycle.

28 September 2017

1 reference

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Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.

31 May 2018

1 reference

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Müllerian agenesis: an update

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

Vaginal agenesis (Mayer-Rokitansky-Kuster-Hauser syndrome) associated with the N314D mutation of galactose-1-phosphate uridyl transferase (GALT).

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

The spectrum of congenital anomalies of the VATER association: an international study.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

Hearing loss and the Mayer-Rokitansky-Küster-Hauser syndrome.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

Mayer-Rokitansky-Küster-Hauser syndrome: distinction between two forms based on excretory urographic, sonographic, and laparoscopic findings.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

Gonadal and müllerian duct agenesis in a girl with 46,X,i(Xq).

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

A case of utero-vaginal aplasia with polycystic kidney and mosaic XX=XXX

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

Anomalies of the Vas Deferens

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

Cytogenetics of fifty patients with primary amenorrhea

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

Müllerian tract abnormalities and associated auditory defects.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

Oculo-auriculo-vertebral complex and uncommon associated anomalies: report on 8 unrelated Brazilian patients

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

Congenital absence of the uterus. Clinicopathologic and endocrine findings

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

A community of human malformation syndromes involving the müllerian ducts, distal extremities, urinary tract, and ears

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

XO-XX Mosaicism in the Rokitansky-Kuster-Hauser syndrome.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

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

31 May 2018

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-5-1

Mayer-Rokitansky-Küster-Hauser anomaly and its associated malformations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-5-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-5-1

Congenital absence of the uterus and vagina is not commonly transmitted as a dominant genetic trait: outcomes of surrogate pregnancies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-5-1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-5-1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-5-1

Abdominal B (AbdB) Hoxa genes: regulation in adult uterus by estrogen and progesterone and repression in müllerian duct by the synthetic estrogen diethylstilbestrol (DES).

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-5-1

Haploinsufficiency of the HOXA gene cluster, in a patient with hand-foot-genital syndrome, velopharyngeal insufficiency, and persistent patent Ductus botalli

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-5-1

Dominantly inherited renal adysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-5-1

Exclusion ofWNT4 as a major gene in Rokitansky-Küster-Hauser anomaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-5-1

Extending the scope of the VATER association: definition of the VATER syndrome

21 January 2018

2 references

https://api.crossref.org/works/10.1186%2F1477-5751-5-1

21 January 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

Wnt-7a maintains appropriate uterine patterning during the development of the mouse female reproductive tract.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

Azoospermia and segmentation abnormalities of the cervicothoracic spine ('MURCS in the male').

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

Gene dosage-dependent effects of the Hoxa-13 and Hoxd-13 mutations on morphogenesis of the terminal parts of the digestive and urogenital tracts.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1368996

Role for anti-Müllerian hormone in congenital absence of the uterus and vagina

28 November 2018

1 reference

12 December 2020

MURCS association with duplicated thumb

1 reference

12 December 2020

Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser syndrome in a girl with 46,X,del(X)(pter-->q22:)

1 reference

12 December 2020

High prevalence of müllerian anomalies diagnosed by ultrasound in women with polycystic ovaries

1 reference

12 December 2020

Cytogenetic findings in patients with congenital absence of the vagina

1 reference

12 December 2020

Abnormalities of urinary tract and skeleton associated with congenital absence of vagina

1 reference

12 December 2020

Familial müllerian agenesis

1 reference

12 December 2020

Congenital absence of the vagina. Observations on 25 cases

1 reference

12 December 2020

A second family with renal, vaginal, and middle ear anomalies

1 reference

12 December 2020

Familial occurrence of congenital absence of the vagina

1 reference

12 December 2020

Cyclical Ovarian Function in Women with Congenital Absence of the Uterus and Vagina

1 reference

12 December 2020

Absent Vas Deferens Associated With Renal Agenesis

1 reference

12 December 2020

Congenital anomalies of the upper urinary tract associated with esophageal atresia and tracheoesophageal fistula

1 reference

12 December 2020

Müllerian duct agenesis associated with renal and skeletal abnormalities

1 reference

12 December 2020

Thalidomide and female genital malformations

1 reference

12 December 2020

Hereditary urogenital adysplasia

1 reference

12 December 2020

Vaginal agenesis in association with gonadal dysgenesis

1 reference

12 December 2020

Vaginal malformations

1 reference

12 December 2020

Heritable aspects of uterine anomalies. II. Genetic analysis of Müllerian aplasia

1 reference

12 December 2020

Müllerian anomalies and renal agenesis: autosomal dominant urogenital adysplasia

1 reference

12 December 2020

The concurrence of facioauriculovertebral spectrum and the Rokitansky syndrome

1 reference

12 December 2020

Syndrome of genital, renal, and middle ear anomalies: a third family and report of a pregnancy

1 reference

12 December 2020

Evaluation of radiographic abnormalities of the hand in patients with the Mayer-Rokitansky-Küster-Hauser syndrome

1 reference

12 December 2020

Vaginal atresia (von Mayer-Rokitansky-Küster or MRK anomaly) in hereditary renal adysplasia (HRA)

1 reference

12 December 2020

The MURCS association

1 reference

12 December 2020

A familial syndrome of renal, genital, and middle ear anomalies

1 reference

12 December 2020

Mayer-Rokitansky-Küster-Hauser syndrome and ovarian cancer. Report of a case

1 reference

12 December 2020

Polycystic ovaries in association with müllerian anomalies

1 reference

12 December 2020

Abnormal uterine stromal and glandular function associated with maternal reproductive defects in Hoxa-11 null mice

1 reference

12 December 2020

Tumor in ectopic omental ovary in Mayer-Rokitansky-Küster-Hauser syndrome: CT findings

1 reference

12 December 2020

Gonadal dysgenesis and Rokitansky syndrome. A case report

1 reference

12 December 2020

Unicornuate uterus with a rudimentary horn and ovarian dysgerminoma. A case report

1 reference

12 December 2020

The effect of a group programme on women with the Mayer-Rokitansky-Küster-Hauser syndrome

1 reference

12 December 2020

The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome without and with associated features: two separate entities?

1 reference

12 December 2020

MURCS in a male: a further case

1 reference

12 December 2020

Superovulation-induced intrauterine growth retardation in mice

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-5-1

7 January 2021

inferred from DOI database lookup

The effect of chronic gonadotropin-releasing hormone analog (D-Trp-6) treatment on elevated and normal serum prolactin levels

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-5-1

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1186/1477-5751-5-1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16441882%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

16 January 2020

1 reference

https://scigraph.springernature.com/pub.10.1186/1477-5751-5-1

9 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16441882%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

PubMed publication ID

16441882

1 reference