Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome (Q21203017)

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27 December 2019

review article

1 reference

title

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17359527%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

1 reference

9 October 2019

1 reference

4

Daniel Guerrier

Daniel

Guerrier

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17359527%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

Karine Morcel

1

Karine

Morcel

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17359527%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

Laure Camborieux

series ordinal

2

author given names

Laure

author last names

Camborieux

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17359527%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

Programme de Recherches sur les Aplasies Müllériennes

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17359527%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

language of work or name

English

0 references

publication date

14 March 2007

2 references

9 October 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17359527%20AND%20SRC:MED&resulttype=core&format=json

Orphanet Journal of Rare Diseases

27 December 2019

published in

2 references

9 October 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17359527%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

volume

2

1 reference

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27 December 2019

issue

1

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page(s)

13

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Creative Commons Attribution 2.0 Generic

27 December 2019

copyright license

1 reference

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

9 October 2019

0 references

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney disease

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Vaginoplasty with Interceed absorbable adhesion barrier for complete squamous epithelialization in vaginal agenesis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Female development in mammals is regulated by Wnt-4 signalling

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Use of Interceed Absorbable Adhesion Barrier for vaginoplasty

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Phenotypic variability of a 4q34-->qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Testicular anti-Müllerian hormone: history, genetics, regulation and clinical applications.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Mullerian agenesis and thrombocytopenia absent radius syndrome: a case report and review of syndromes associated with Mullerian agenesis

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Mullerian duct anomalies: imaging and clinical issues

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Developmental genetics of the female reproductive tract in mammals

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Congenital malformations of the genital tract and their management

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Tetralogy of Fallot, imperforate anus, and Müllerian, renal, and cervical spine (MURCS) anomalies in a 15-year-old girl

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Disorders of androgen action

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patients

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Wnts and the female reproductive system.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Vaginal creation for müllerian agenesis

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Müllerian agenesis: etiology, diagnosis, and management

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Genetics of the female reproductive ducts

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Cell lineages in the embryonic kidney: their inductive interactions and signalling molecules

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

The Vecchietti procedure for surgical treatment of vaginal agenesis: comparison of laparoscopy and laparotomy

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Chromosome 22q11 deletion presenting as the Potter sequence

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

MURCS association: case report and review

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Congenital anomalies of the müllerian system

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Stapedial ankylosis in the Mayer-Rokitansky-Küster-Hauser syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Roles of growth factors in renal development.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Müllerian agenesis: an update

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Success following vaginal creation for Müllerian agenesis.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Anomalies of the Vas Deferens

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Cytogenetics of fifty patients with primary amenorrhea

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Absent vagina and the Klippel-Feil anomaly.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Phocomelia and additional anomalies in two sisters.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Müllerian duct anomalies: MR imaging evaluation

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Müllerian tract abnormalities and associated auditory defects.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Spinal abnormalities and the atypical form of the Mayer-Rokitansky-Küster-Hauser syndrome

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Congenital absence of the uterus. Clinicopathologic and endocrine findings

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Report of a del22q11 in a patient with Mayer-Rokitansky-Küster-Hauser (MRKH) anomaly and exclusion ofWNT-4,RAR-gamma, andRXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Monozygotic twins discordant for vaginal agenesis and bilateral tibial longitudinal deficiency

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Essential function of Wnt-4 for tubulogenesis in the Xenopus pronephric kidney.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

ACOG Committee Opinion. Number 274, July 2002. Nonsurgical diagnosis and management of vaginal agenesis.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Epidemiological analysis of outcomes of pregnancy in gestational diabetic mothers

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Epidemiological analysis of outcomes of pregnancy in diabetic mothers: identification of the most characteristic and most frequent congenital anomalies

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Dominantly inherited renal adysplasia

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1832178

Gonadal agenesis 46,XX associated with the atypical form of Rokitansky syndrome

29 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

Mayer-Rokitansky-Küster-Hauser syndrome associated with unilateral gonadal agenesis. A case report

1 reference

12 December 2020

Facio-auriculo-vertebral sequence in association with DiGeorge sequence, Rokitansky sequence, and Dandy-Walker malformation: case report

1 reference

12 December 2020

Mayer-von Rokitansky-Küster-Hauser syndrome in association with a hitherto undescribed variant of the Holt-Oram syndrome with an aorto-pulmonary window

1 reference

12 December 2020

Mayer-Rokitansky-Küster-Hauser syndrome associated with pulmonary stenosis

1 reference

12 December 2020

Cytogenetic findings in patients with congenital absence of the vagina

1 reference

12 December 2020

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

1 reference

12 December 2020

Congenital absence of the vagina. Observations on 25 cases

1 reference

12 December 2020

[Rokitansky-Kuster-Hauser and similar syndromes of uter-vaginal aplasia]

1 reference

12 December 2020

[Colpopoeisis from the peritoneum of the uterorectal space]

1 reference

12 December 2020

Familial occurrence of congenital absence of the vagina

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

Concurrence of the Holt-Oram syndrome and the Rokitansky-Kuster-Hauser syndrome. A case report

1 reference

12 December 2020

Rokitansky-Küster-Hauser syndrome with ectrodactyly

1 reference

12 December 2020

A modified technique to create a neovagina with an isolated segment of sigmoid colon

1 reference

12 December 2020

Hereditary urogenital adysplasia

1 reference

12 December 2020

The bicycle seat stool in the treatment of vaginal agenesis and stenosis: A preliminary report

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

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

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

[Value of ultrasonography in utero-vaginal aplasia]

1 reference

12 December 2020

[Gynecological malformations. Classification and contribution of different imaging methods]

1 reference

12 December 2020

Creation of a sigmoid neovagina: technique and results in 16 cases

1 reference

12 December 2020

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

1 reference

12 December 2020

MURCS in a male: a further case

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

Thalidomide and female genital malformations

1 reference

12 December 2020

[Pure gonadal dysgenesis XX and XY: observations in fifteen patients]

1 reference

12 December 2020

Primary amenorrhea in a teenager

1 reference

12 December 2020

Hereditary renal adysplasia in a three generations family

1 reference

12 December 2020

Gonadal dysgenesis and Rokitansky syndrome. A case report

1 reference

12 December 2020

Rokitansky syndrome and MURCS association--clinical features and basis for diagnosis

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

Familial müllerian agenesis

1 reference

12 December 2020

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

1 reference

12 December 2020

Renal abnormalities in Mayer-Rokitanski-Küster-Hauser syndrome

1 reference

12 December 2020

Hepatocyte nuclear factor-1beta: a new kindred with renal cysts and diabetes and gene expression in normal human development

1 reference

12 December 2020

[Mayer-Rokitansky-Kuster-Hauser syndrome: associated pathologies]

1 reference

12 December 2020

Identifiers

DOI

10.1186/1750-1172-2-13

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

377978

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17359527%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

27 December 2019

1006874635

0 references

OpenCitations bibliographic resource ID

377978

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17359527%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

1 reference