(Q50307316)

2 March 2018

title

Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder. (English)

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2 March 2018

main subject

autism spectrum disorder

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Martin Poot

1

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2 March 2018

Vera Beyer

2

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2 March 2018

Ira Schwaab

3

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2 March 2018

Natalja Damatova

4

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2 March 2018

Ruben Van't Slot

5

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2 March 2018

Jo Prothero

6

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2 March 2018

Sue E Holder

7

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2 March 2018

Thomas Haaf

8

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2 March 2018

publication date

7 July 2009

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2 March 2018

published in

Neurogenetics

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2 March 2018

volume

11

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2 March 2018

issue

1

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2 March 2018

page(s)

81-89

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2 March 2018

https://scigraph.springernature.com/pub.10.1007/s10048-009-0205-1

exact match

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cites work

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome.

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12 December 2020

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12 December 2020

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12 December 2020

A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea

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A microhomology-mediated break-induced replication model for the origin of human copy number variation

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12 December 2020

10.1007/S10048-009-0205-1

Identifiers

DOI

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2 March 2018

PubMed ID

19582487

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2 March 2018