(Q34715118)

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Syndromes with cephaloceles

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PubMed publication ID

7101196

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4 August 2017

title

Syndromes with cephaloceles (English)

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PubMed publication ID

4 August 2017

Cohen MM Jr

1

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PubMed publication ID

7101196

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4 August 2017

Lemire RJ

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2

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7101196

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4 August 2017

publication date

1 April 1982

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4 August 2017

published in

Birth Defects Research Part A: Clinical and Molecular Teratology

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7101196

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4 August 2017

volume

25

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7101196

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4 August 2017

issue

2

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7101196

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4 August 2017

page(s)

161-172

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7101196

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cites work

The median cleft face syndrome: Differential diagnosis of cranium bifidum occultum, hypertelorism, and median cleft nose, lip, and palate

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Crossref

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https://api.crossref.org/works/10.1002%2FTERA.1420250206

retrieved

21 January 2018

1977 Edward B. D. Neuhauser lecture: neurofibromatosis in children

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https://api.crossref.org/works/10.1002%2FTERA.1420250206

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21 January 2018

The syndrome of basal encephalocele and hypothalamic-pituitary dysfunction

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reference URL

https://api.crossref.org/works/10.1002%2FTERA.1420250206

retrieved

21 January 2018

Ocular Manifestations of the Meckel Syndrome

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reference URL

https://api.crossref.org/works/10.1002%2FTERA.1420250206

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21 January 2018

PARIETAL CEPHALOCELES.

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reference URL

https://api.crossref.org/works/10.1002%2FTERA.1420250206

retrieved

21 January 2018

Identifiers

DOI

10.1002/TERA.1420250206

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7101196

retrieved

4 August 2017

PubMed publication ID

7101196

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7101196

retrieved

4 August 2017

(Q34715118)

Syndromes with cephaloceles

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