(Q41635606)

English

The McKusick-Kaufman syndrome: Recessively inherited vaginal atresia, hydrometrocolpos, uterovaginal duplications, anorectal anomalies, postaxial polydactyly, and congenital heart disease

scientific article published on May 1, 1979

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

The McKusick-Kaufman syndrome: recessively inherited vaginal atresia, hydrometrocolpos, uterovaginal duplications, anorectal anomalies, postaxial polydactyly, and congenital heart disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A448491

2 July 2022

The McKusick-Kaufman syndrome: Recessively inherited vaginal atresia, hydrometrocolpos, uterovaginal duplications, anorectal anomalies, postaxial polydactyly, and congenital heart disease (English)

1 reference

10.1016/S0022-3476(79)80155-9

https://api.crossref.org/works/10.1016/S0022-3476(79)80155-9

16 May 2023

congenital disorder

0 references

1 reference

based on heuristic

inferred from title

postaxial polydactyly

1 reference

based on heuristic

inferred from title

McKusick–Kaufman syndrome

1 reference

based on heuristic

inferred from title

multiple abnormalities

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A448491

2 July 2022

author name string

M. Robinow

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A448491

2 July 2022

A. Shaw

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A448491

2 July 2022

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publication date

1 May 1979

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

full work available at URL

https://api.elsevier.com/content/article/PII:S0022347679801559?httpAccept=text/xml

1 reference

10.1016/S0022-3476(79)80155-9

https://api.crossref.org/works/10.1016/S0022-3476(79)80155-9

16 May 2023

https://api.elsevier.com/content/article/PII:S0022347679801559?httpAccept=text/plain

1 reference

10.1016/S0022-3476(79)80155-9

https://api.crossref.org/works/10.1016/S0022-3476(79)80155-9

16 May 2023

The Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

94

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

776-778

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

HYDROMETROCOLPOS AS A SIMPLY INHERITED MALFORMATION.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980155-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980155-9

7 January 2021

CONGENITAL HYDROCOLPOS

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980155-9

7 January 2021

Hydrometrocolpos in infancy

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980155-9

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2879%2980155-9

7 January 2021

Identifiers

10.1016/S0022-3476(79)80155-9

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 October 2017

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