Structural variation of chromosomes in autism spectrum disorder (Q24656970)

Dalila Pinto

9

0 references

Can Ficicioglu

Can Ficicioglu

17

0 references

Jan M Friedman

Jan Friedman

14

0 references

Peter Szatmari

34

Peter Szatmari

0 references

Stephen W. Scherer

35

Stephen W Scherer

0 references

Anne O. Summers

21

Anne Summers

0 references

Wendy Roberts

32

Wendy Roberts

0 references

Lars Feuk

5

Lars Feuk

0 references

Stefan Schreiber

13

Stefan Schreiber

0 references

Rosanna Weksberg

25

Rosanna Weksberg

0 references

Anath C. Lionel

4

Anath C Lionel

0 references

Bridget A. Fernandez

33

Bridget Fernandez

0 references

Christian Marshall

1

Christian R Marshall

0 references

Andreas Fiebig

12

Andreas Fiebig

0 references

Rainald Moessner

8

Rainald Moessner

0 references

Jennifer Skaug

6

Jennifer Skaug

0 references

Mary Shago

7

Bhooma Thiruvahindrapduram

Mary Shago

0 references

11

Bhooma Thiruvahindrapduram

0 references

Cathy Vardy

27

Cathy Vardy

0 references

Sandra Luscombe

29

Sandra Luscombe

0 references

Rob Nicolson

19

Rob Nicolson

0 references

author name string

Abdul Noor

2

0 references

John B Vincent

3

0 references

Yan Ren

10

0 references

Cees E J Ketelaars

15

0 references

Yvonne J Vos

16

0 references

Susan Kirkpatrick

18

0 references

Leon Sloman

20

0 references

Clare A Gibbons

22

0 references

Ahmad Teebi

23

0 references

David Chitayat

24

0 references

Ann Thompson

26

0 references

Vicki Crosbie

28

0 references

Rebecca Baatjes

American Journal of Human Genetics

30

0 references

language of work or name

English

0 references

publication date

February 2008

0 references

published in

0 references

volume

82

0 references

issue

2

0 references

page(s)

477-88

0 references

cites work

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7 April 2017

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Dissection of synapse induction by neuroligins: effect of a neuroligin mutation associated with autism

7 April 2017

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7 April 2017

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7 April 2017

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7 April 2017

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28 September 2017

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28 November 2018

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28 November 2018

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A novel microdeletion at 16p11.2 harbors candidate genes for aortic valve development, seizure disorder, and mild mental retardation

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18252227

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18252227

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Molecular Cytogenetics of Autism

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FJ.AJHG.2007.12.009

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2007.12.009

1 reference

1215553

1215553

1 reference

1 reference

1 reference