(Q50303118)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23279911%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

title

A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features (English)

1 reference

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21 February 2020

1 reference

microdeletion syndrome

1 reference

18

1 reference

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21 February 2020

Ann-Charlotte Thuresson

16

1 reference

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21 February 2020

13

Helen Firth

1 reference

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21 February 2020

15

Joris Vermeesch

1 reference

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21 February 2020

17

Henri Copin

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23279911%20AND%20SRC:MED&resulttype=core&format=json

21 February 2020

author name string

Elise Boudry-Labis

1

1 reference

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21 February 2020

Bénédicte Demeer

2

1 reference

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21 February 2020

Cédric Le Caignec

3

1 reference

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21 February 2020

Bertrand Isidor

4

1 reference

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21 February 2020

Michèle Mathieu-Dramard

5

1 reference

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21 February 2020

Ghislaine Plessis

6

1 reference

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21 February 2020

Alice M George

7

1 reference

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21 February 2020

Juliet Taylor

8

1 reference

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21 February 2020

Salim Aftimos

9

1 reference

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21 February 2020

Adelheid Wiemer-Kruel

10

1 reference

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21 February 2020

Jürgen Kohlhase

11

1 reference

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21 February 2020

Göran Annerén

12

1 reference

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21 February 2020

Ingrid Simonic

14

1 reference

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21 February 2020

Joris Andrieux

19

1 reference

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21 February 2020

publication date

29 December 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23279911%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Medical Genetics

21 February 2020

published in

1 reference

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21 February 2020

volume

56

1 reference

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21 February 2020

issue

3

1 reference

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21 February 2020

page(s)

163-170

1 reference