(Q87242657)

English

X chromosome exome sequencing reveals a novel ALG13 mutation in a nonsyndromic intellectual disability family with multiple affected male siblings

scientific article published on 01 January 2014

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24501762%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

X chromosome exome sequencing reveals a novel ALG13 mutation in a nonsyndromic intellectual disability family with multiple affected male siblings (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24501762%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

intellectual disability

1 reference

based on heuristic

inferred from title

disability affecting intellectual abilities

1 reference

based on heuristic

inferred from title

non-syndromic intellectual disability

1 reference

based on heuristic

inferred from title

Stanley F Nelson

4

object named as

Stanley F Nelson

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24501762%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

author name string

Nesrine Bissar-Tadmouri

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24501762%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

Whithey L Donahue

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24501762%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

Lihadh Al-Gazali

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24501762%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

Pinar Bayrak-Toydemir

5

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24501762%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

Sibel Kantarci

6

1 reference

Europe PubMed Central

PubMed publication ID

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7 March 2020

publication date

1 January 2014

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24501762%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

American Journal of Medical Genetics

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24501762%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

164A

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7 March 2020

1

1 reference

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PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24501762%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

164-169

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24501762%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

Identifiers

10.1002/AJMG.A.36233

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24501762%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24501762%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

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