(Q57924143)

English

Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations

scientific article published on 01 July 2003

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12794692%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12794692%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Greig cephalopolysyndactyly syndrome

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based on heuristic

inferred from title

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based on heuristic

inferred from title

author name string

Philippe Debeer

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12794692%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

H Peeters

2

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4 November 2019

S Driess

3

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4 November 2019

L De Smet

4

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4 November 2019

K Freese

5

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4 November 2019

G Matthijs

6

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4 November 2019

D Bornholdt

7

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4 November 2019

K Devriendt

8

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4 November 2019

K-H Grzeschik

9

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4 November 2019

J-P Fryns

10

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4 November 2019

M Kalff-Suske

11

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4 November 2019

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publication date

1 July 2003

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4 November 2019

American Journal of Medical Genetics

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4 November 2019

120A

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4 November 2019

1

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4 November 2019

49-58

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4 November 2019

Identifiers

10.1002/AJMG.A.20018

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Europe PubMed Central

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4 November 2019

PubMed publication ID

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4 November 2019

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