E. Mickelson

发表

Screening for Autism Spectrum Disorders With the Social Communication Questionnaire

L. Eaves, H. Wingert, H. Ho, 2006, Journal of developmental and behavioral pediatrics : JDBP.

Diagnosis and management of developmental coordination disorder

J. Zwicker, S. Harris, E. Mickelson, 2015, Canadian Medical Association Journal.

A variant Cri du Chat phenotype and autism spectrum disorder in a subject with de novo cryptic microdeletions involving 5p15.2 and 3p24.3‐25 detected using whole genomic array CGH

E. Mickelson, E. Rajcan-Separovic, J. Holden, 2005, Clinical genetics.

Association of GTF2i in the Williams-Beuren Syndrome Critical Region with Autism Spectrum Disorders

I. Cohen, A. Chudley, J. Holden, 2011, Journal of Autism and Developmental Disorders.

Association of GTF2i in the Williams-Beuren Syndrome Critical Region with Autism Spectrum Disorders

I. Cohen, A. Chudley, J. Holden, 2011, Journal of Autism and Developmental Disorders.

15q Duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array‐CGH

M. V. Van Allen, H. Wingert, E. Mickelson, 2006, Clinical genetics.

Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1

E. Mickelson, B. McGillivray, J. Hall, 2006, Journal of Medical Genetics.

The Value of a Genetic Diagnosis for Individuals with Intellectual Disabilities: Optimising Healthcare and Function Across the Lifespan

E. Mickelson, E. Lopez-Rangel, M. S. Suzanne Lewis, 2008 .

Assessment, diagnosis, and management of developmental coordination disorder.

J. Zwicker, E. Mickelson, A. Ip, 2021, Paediatrics & child health.