(Q38007768)

English

De novo microdeletions of chromosome 6q14.1-q14.3 and 6q12.1-q14.1 in two patients with intellectual disability - further delineation of the 6q14 microdeletion syndrome and review of the literature.

scientific article published on 12 April 2012

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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:22561202%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

De novo microdeletions of chromosome 6q14.1-q14.3 and 6q12.1-q14.1 in two patients with intellectual disability - further delineation of the 6q14 microdeletion syndrome and review of the literature (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22561202%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

0 references

intellectual disability

1 reference

based on heuristic

inferred from title

microdeletion syndrome

1 reference

based on heuristic

inferred from title

disability affecting intellectual abilities

1 reference

based on heuristic

inferred from title

Nataliya Di Donato

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22561202%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

Ann-Charlotte Thuresson

10

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31 January 2020

13

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31 January 2020

16

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31 January 2020

Muriel Holder-Espinasse

3

object named as

Muriel Holder-Espinasse

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31 January 2020

4

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Joris Andrieux

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31 January 2020

9

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Bruno Delobel

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31 January 2020

author name string

Kerstin Becker

1

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31 January 2020

Jean-Marie Cuisset

5

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31 January 2020

Louis Vallée

6

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31 January 2020

Ghislaine Plessis

7

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31 January 2020

Nolwenn Jean

8

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Europe PubMed Central

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31 January 2020

Göran Annerén

11

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Europe PubMed Central

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31 January 2020

Kirstine Ravn

12

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31 January 2020

Sigrid Tinschert

14

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Europe PubMed Central

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31 January 2020

Evelin Schrock

15

1 reference

Europe PubMed Central

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31 January 2020

Karl Hackmann

17

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31 January 2020

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publication date

12 April 2012

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31 January 2020

European Journal of Medical Genetics

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31 January 2020

55

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31 January 2020

8-9

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31 January 2020

490-497

1 reference

Europe PubMed Central

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31 January 2020

The influence of serotonin- and other genes on impulsive behavioral aggression and cognitive impulsivity in children with attention-deficit/hyperactivity disorder (ADHD): Findings from a family-based association test (FBAT) analysis

1 reference

5 May 2024

https://opencitations.net/index/api/v1/citations/10.1186/1744-9081-4-48

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

1 reference

5 May 2024

https://opencitations.net/index/api/v1/citations/10.1002/AJMG.B.30867

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