(Q33869559)

29 July 2017

1 reference

title

Genetics of the female reproductive ducts (English)

1 reference

29 July 2017

Simpson JL

1

1 reference

PubMed ID

10727998

29 July 2017

language of work or name

1 reference

1 December 1999

1 reference

American Journal of Medical Genetics Part A

29 July 2017

1 reference

29 July 2017

89

1 reference

29 July 2017

4

1 reference

29 July 2017

224-239

1 reference

The Schinzel-Giedion syndrome

29 July 2017

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Robinow syndrome, vaginal atresia, hematocolpos, and extra middle finger

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Spondylocostal dysostosis associated with anal and urogenital anomalies in a Mennonite sibship

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Visceral anomalies in the Apert syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Sonographic and urographic correlation in Bardet-Biedl syndrome (formerly Laurence-Moon-Biedl syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Ovarian dysgenesis in individuals with chromosomal abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

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/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

A recessive mutation causing imperforate vagina in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Antley-Bixler syndrome from a prognostic perspective: report of a case and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

The newly recognised limb/pelvis-hypoplasia/aplasia syndrome: report of a Bedouin patient and review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Reconstructive surgery for congenital atresia of the uterine cervix.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Fryns syndrome: a variable MCA syndrome with diaphragmatic defects, coarse face, and distal limb hypoplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

A new lethal syndrome with cloudy corneae, diaphragmatic defects and distal limb deformities

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Congenital cervical atresia: report of seven cases and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Johanson-Blizzard syndrome: clinical spectrum and further delineation of the syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

The hand-foot-genital (hand-foot-uterus) syndrome: family report and update

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Limb pterygium syndromes: a review and report of eleven patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus and postaxial polydactyly--a new syndrome? Part I: clinical, causal, and pathogenetic considerations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Congenital abnormalities of the uterus and pregnancy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

A syndrome of congenital aplasia of the alae nasi, deafness, hypothyroidism, dwarfism, absent permanent teeth, and malabsorption

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Salvage of the reproductive potential of women with anomalous development of the Müllerian ducts: 1868-1968-2068

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland. Clinical, genetic and epidemiological studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Three new cases of the Schinzel-Giedion syndrome and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Female pseudohermaphroditism and associated anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Recessive inheritance of a congenital malformation syndrome: unilateral absence deformity of leg and congenital cataracts

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Pathology of Laurence-Moon-Bardet-Biedl syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Mutation of HOXA13 in hand-foot-genital syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

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/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Nonskeletal malformations in one of three siblings with Jarcho-Levin syndrome of vertebral anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Severe developmental failure with coarse facialfeatures, distal limb hypoplasia, thickened palmar creases, bifid uvula, and ureteral stenosis: A previously unidentified familial disorder with lethal outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

21 January 2018

Hydrolethalus syndrome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Bardet-Biedl syndrome and related disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Phocomelia and additional anomalies in two sisters.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Antley-Bixler syndrome in sisters: a term newborn and a prenatally diagnosed fetus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

A syndrome of severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations in sibs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Ovarian differentiation and gonadal failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

The hand-food-uterus syndrome: a new hereditary disorder characterized by hand and foot dysplasia, dermatoglyphic abnormalities, and partial duplication of the female genital tract

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Genital abnormalities in females with Bardet-Biedl syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Genetic and physical mapping of the McKusick-Kaufman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Autosomal recessive Robinow syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Limb/pelvis/uterus-hypoplasia/aplasia syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Pallister-Hall syndrome and McKusick-Kaufmann syndrome: one entity?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Roberts syndrome: a review of 100 cases and a new rating system for severity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

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/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

The syndrome of caudal dysplasia: a review, including etiologic considerations and evidence of heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Diagnostic problems in a case with mucometrocolpos, polydactyly, congenital heart disease, and skeletal dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Acrocephalosyndactyly (Apert's Syndrome): Temporal Bone Findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Dominantly inherited renal adysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Congenital absence of the vagina. Long-term results of vaginal reconstruction in 175 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Update on a family with hand-foot-genital syndrome: hypospadias and urinary tract abnormalities in two boys from the fourth generation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Three sisters with septate uteri: another reference to bidirectional theory

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Syndromic forms of hydrometrocolpos

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

The hand-foot-genital syndrome: on the variable expression in affected males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Hand-foot-uterus-(HFU) syndrome with hypospadias: the hand-foot-genital- (HFG) syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Gonadal dysgenesis and gonadoblastoma in situ in a female with Fraser (cryptophthalmos) syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

A new syndrome of severe upper limb hypoplasia and Müllerian duct anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Acro-renal-mandibular syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Uterus unicollis and its relationship to pregnancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Thalidomide and female genital malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

The Wolf-Hirschhorn (4p-) syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Familial occurrence of congenital absence of the vagina

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Nature of the obstructing membrane in primary cryptomenorrhoea

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Unusual malformation of the uterus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Congenital absence of the vagina. Observations on 25 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

HYDROMETROCOLPOS AS A SIMPLY INHERITED MALFORMATION.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Trisomy 7 and Potter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819991229%2989%3A4%3C224%3A%3AAID-AJMG7%3E3.0.CO%3B2-C

Visceral anomalies in the Meckel syndrome

21 January 2018

1 reference

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Prune belly syndrome in females: a triad of abdominal musculature deficiency and anomalies of the urinary and genital systems

21 January 2018

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Polyasplenia, caudal deficiency, and agenesis of the corpus callosum

21 January 2018

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The hydrolethalus syndrome: delineation of a "new", lethal malformation syndrome based on 28 patients.

21 January 2018

1 reference

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Female pseudohermaphroditism with multiple caudal anomalies: absence of Y-specific DNA sequences as pathogenetic factors

21 January 2018

1 reference

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Observations on the results of pregnancies in women resident in Belfast. II. Abortions, hydatidiform moles and ectopic pregnancies

21 January 2018

1 reference

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Leprechaunism (Donohue's syndrome): Acase report

21 January 2018

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Nosology of Smith-Lemli-Opitz syndrome

21 January 2018

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Spinal Changes in Patients with Congenital Aplasia of the Vagina

21 January 2018

1 reference

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Heritable aspects of uterine anomalies. I. Three familial aggregates with Müllerian fusion anomalies

21 January 2018

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Urinary tract abnormalities in hand-foot-genital syndrome

21 January 2018

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The concurrence of facioauriculovertebral spectrum and the Rokitansky syndrome

21 January 2018

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

21 January 2018

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Full trisomy 7 and Potter syndrome

21 January 2018

1 reference

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10.1002/(SICI)1096-8628(19991229)89:4<224::AID-AJMG7>3.0.CO;2-C

21 January 2018

Identifiers

DOI

1 reference

29 July 2017

1 reference

PubMed ID

10727998