Hirschsprung disease in a 46,XY phenotypic infant girl with Smith-Lemli-Opitz syndrome (Q34713837)

4 August 2017

title

Hirschsprung disease in a 46,XY phenotypic infant girl with Smith-Lemli-Opitz syndrome (English)

1 reference

4 August 2017

Patterson K

1

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4 August 2017

Toomey KE

series ordinal

2

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4 August 2017

Chandra RS

series ordinal

3

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4 August 2017

language of work or name

English

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publication date

1 September 1983

1 reference

The Journal of Pediatrics

4 August 2017

published in

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4 August 2017

volume

103

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4 August 2017

issue

3

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4 August 2017

page(s)

425-427

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A NEWLY RECOGNIZED SYNDROME OF MULTIPLE CONGENITAL ANOMALIES.

4 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980422-3

Micrognathia, polydactyly, and cleft palate

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980422-3

Borderline normal intelligence in the Smith-Lemli-Opitz (RSH) syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980422-3

Ocular Manifestations of the Smith-Lemli-Opitz Syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2883%2980422-3

10.1016/S0022-3476(83)80422-3

7 January 2021

Identifiers

DOI

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4 August 2017

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