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Kirsty Wing

Showing results (1-10 of 10) with videos related to

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Journal of Neurodevelopmental Disorders|April 13, 2011
A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3Alistair T Pagnamenta, Richard Holt, Mohammed Yusuf, et al.
Diseases of the Colon and Rectum|February 8, 2020
International Consensus Definition of Low Anterior Resection SyndromeCelia Keane, Nicola S Fearnhead, Liliana G Bordeianou, et al.
ANZ Journal of Surgery|February 11, 2020
International consensus definition of low anterior resection syndromeCelia Keane, Nicola S Fearnhead, Liliana G Bordeianou, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
A 15q13.3 microdeletion segregating with autismAlistair T Pagnamenta, Kirsty Wing, Elham Sadighi Akha, et al.
Journal of Medical Genetics|October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disabilityAlistair T Pagnamenta, Hameed Khan, Susan Walker, et al.
American Journal of Human Genetics|April 29, 2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disordersDalila Pinto, Elsa Delaby, Daniele Merico, et al.
Human Genetics|October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorderJillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.
Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Journal of Neurodevelopmental Disorders|April 13, 2011
A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3Alistair T Pagnamenta, Richard Holt, Mohammed Yusuf, et al.
Diseases of the Colon and Rectum|February 8, 2020
International Consensus Definition of Low Anterior Resection SyndromeCelia Keane, Nicola S Fearnhead, Liliana G Bordeianou, et al.
ANZ Journal of Surgery|February 11, 2020
International consensus definition of low anterior resection syndromeCelia Keane, Nicola S Fearnhead, Liliana G Bordeianou, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
A 15q13.3 microdeletion segregating with autismAlistair T Pagnamenta, Kirsty Wing, Elham Sadighi Akha, et al.
Journal of Medical Genetics|October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disabilityAlistair T Pagnamenta, Hameed Khan, Susan Walker, et al.
American Journal of Human Genetics|April 29, 2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disordersDalila Pinto, Elsa Delaby, Daniele Merico, et al.
Human Genetics|October 15, 2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorderJillian P Casey, Tiago Magalhaes, Judith M Conroy, et al.
Human Molecular Genetics|July 31, 2012
Individual common variants exert weak effects on the risk for autism spectrum disordersRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Human Molecular Genetics|July 29, 2010
A genome-wide scan for common alleles affecting risk for autismRichard Anney, Lambertus Klei, Dalila Pinto, et al.
Nature|June 10, 2010
Functional impact of global rare copy number variation in autism spectrum disordersDalila Pinto, Alistair T Pagnamenta, Lambertus Klei, et al.
Pageof 1