Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria-Reference-Cited by-同舟云学术

Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria

Published:2013-08-05 Issue:9 Volume:161 Page:2321-2326
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Turner Samantha J¹,Hildebrand Michael S.²,Block Susan³,Damiano John²,Fahey Michael⁴,Reilly Sheena¹⁵,Bahlo Melanie⁶⁷,Scheffer Ingrid E.¹²⁸,Morgan Angela T.¹⁵

Affiliation:

1. Department of Paediatrics, The Royal Children's Hospital; The University of Melbourne; Parkville Victoria Australia

2. Department of Medicine; The University of Melbourne, Austin Health; Heidelberg Victoria Australia

3. Department of Human Communication Sciences; La Trobe University; Bundoora Victoria Australia

4. Department of Paediatrics; Monash University; Clayton Victoria Australia

5. Population Health, Genes and Environment Theme; Murdoch Childrens Research Institute; Parkville Victoria Australia

6. Bioinformatics Division; The Walter and Eliza Hall Institute of Medical Research; Parkville Victoria Australia

7. Department of Mathematics and Statistics; The University of Melbourne; Parkville Victoria Australia

8. Florey Institute; Melbourne Victoria Australia

Funder

Australian Research Council (ARC) Discovery Project

National Health & Medical Research Council (NHMRC) CJ Martin Overseas Biomedical Postdoctoral Training Fellowship

NHMRC Dora Lush Postgraduate Scholarship

NHMRC Career Development Award

Victorian Government's Operational Infrastructure Support Program ARC Future Fellowship

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36055/fullpdf

Reference37 articles.

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3. American Speech-Language-Hearing Association (ASHA) 2007 http://www.asha.org/policy

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