MG-105 Delineating the phenotypes associated with the 15q11.2 BP1-BP2 deletion: Preliminary trends in psychometric evaluation

Melissa Carter; Bonnie MacKinnon; Sanne Jilderda; Jhoan Falcon; Pooja Swaroop; Breanne Dale; Abdul Noor; Anne S Bassett; Dimitri J Stavropoulos; Irene Drmic

doi:10.1136/jmedgenet-2015-103578.6

Article info

Clinical Genetics

Posters MG-100 to MG-119

MG-105 Delineating the phenotypes associated with the 15q11.2 BP1-BP2 deletion: Preliminary trends in psychometric evaluation

Authors

Melissa Carter 1The Hospital for Sick Children, Toronto, ON, Canada PubMed articles Google scholar articles
Bonnie MacKinnon 2Autism Research Unit, The Hospital for Sick Children, Toronto, ON, Canada PubMed articles Google scholar articles
Sanne Jilderda 2Autism Research Unit, The Hospital for Sick Children, Toronto, ON, Canada PubMed articles Google scholar articles
Jhoan Falcon 2Autism Research Unit, The Hospital for Sick Children, Toronto, ON, Canada PubMed articles Google scholar articles
Pooja Swaroop 2Autism Research Unit, The Hospital for Sick Children, Toronto, ON, Canada PubMed articles Google scholar articles
Breanne Dale 2Autism Research Unit, The Hospital for Sick Children, Toronto, ON, Canada PubMed articles Google scholar articles
Abdul Noor 1The Hospital for Sick Children, Toronto, ON, Canada PubMed articles Google scholar articles
Anne S Bassett 3CAMH, Toronto, ON, Canada PubMed articles Google scholar articles
Dimitri J Stavropoulos 4Genome Diagnostics, The Hospital for Sick Children, Toronto, ON, Canada PubMed articles Google scholar articles
Irene Drmic 1The Hospital for Sick Children, Toronto, ON, Canada PubMed articles Google scholar articles

Citation

Carter M, MacKinnon B, Jilderda S, et al

MG-105 Delineating the phenotypes associated with the 15q11.2 BP1-BP2 deletion: Preliminary trends in psychometric evaluation

Journal of Medical Genetics 2015;52:A2-A3.

Publication history

First published December 4, 2015.

Online issue publication

April 27, 2016

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