(Q45006693)

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The factor V G1691A mutation is a risk for porencephaly: A case-control study

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Europe PubMed Central

PubMed publication ID

8 December 2017

The factor V G1691A mutation is a risk for porencephaly: A case-control study (English)

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Europe PubMed Central

PubMed publication ID

8 December 2017

Ronald Sträter

3

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Ronald Sträter

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Ulrike Nowak-Göttl

5

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Ulrike Nowak-Göttl

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author name string

Otfried M Debus

1

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Europe PubMed Central

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8 December 2017

Andrea Kosch

2

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Europe PubMed Central

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8 December 2017

Ronald Sträter

3

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Europe PubMed Central

PubMed publication ID

8 December 2017

Rainer Rossi

4

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Europe PubMed Central

PubMed publication ID

8 December 2017

Ulrike Nowak-Göttl

5

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Europe PubMed Central

PubMed publication ID

8 December 2017

publication date

1 August 2004

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Europe PubMed Central

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8 December 2017

Annals of Neurology

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8 December 2017

56

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Europe PubMed Central

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8 December 2017

2

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Europe PubMed Central

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8 December 2017

287-290

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Europe PubMed Central

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8 December 2017

Fetal porencephaly: a review of etiology, diagnosis, and prognosis

1 reference

https://api.crossref.org/works/10.1002%2FANA.20184

21 January 2018

Multicentre evaluation of combined prothrombotic defects associated with thrombophilia in childhood. Childhood Thrombophilia Study Group.

1 reference

https://api.crossref.org/works/10.1002%2FANA.20184

21 January 2018

Thromboembolism in children

1 reference

https://api.crossref.org/works/10.1002%2FANA.20184

21 January 2018

Mutations in coagulation factors in women with unexplained late fetal loss.

1 reference

https://api.crossref.org/works/10.1002%2FANA.20184

21 January 2018

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.

1 reference

https://api.crossref.org/works/10.1002%2FANA.20184

21 January 2018

Neuroimaging fails to identify asymptomatic carriers of familial porencephaly

1 reference

https://api.crossref.org/works/10.1002%2FANA.20184

21 January 2018

Identifiers

10.1002/ANA.20184

1 reference

Europe PubMed Central

PubMed publication ID

8 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 December 2017

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