(Q48274707)

10 February 2018

title

A patient with hydranencephaly and PEHO-like dysmorphic features (English)

1 reference

10 February 2018

author

Jean-François Chateil

object named as

Jean-François Chateil

4

0 references

Didier Lacombe

object named as

Didier Lacombe

6

0 references

author name string

Cyril Goizet

1

1 reference

10 February 2018

Caroline Espil-Taris

2

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10 February 2018

Marie Husson

3

1 reference

10 February 2018

Jean-Michel Pedespan

5

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10 February 2018

publication date

1 January 2003

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10 February 2018

published in

Annales de Génétique

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10 February 2018

volume

46

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10 February 2018

issue

1

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10 February 2018

page(s)

25-28

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10 February 2018

Diagnostic criteria and genetics of the PEHO syndrome

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2803%2900003-0

Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome) in two Japanese siblings

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2803%2900003-0

Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2803%2900003-0

Genetic disorders and cerebellar structural abnormalities in childhood

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2803%2900003-0

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2803%2900003-0

PEHO or PEHO-like syndrome?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2803%2900003-0

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0003-3995(03)00003-0

1 reference

10 February 2018

release_uxqlox2kyfhq7hm56m4b7ktgza

Fatcat ID

0 references

1 reference

10 February 2018