Phenotypic and Evolutionary Consequences of Deletion, Duplication, and Triplication at 16p11.2-Reference-Cited by-同舟云学术

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Phenotypic and Evolutionary Consequences of Deletion, Duplication, and Triplication at 16p11.2

Published:2018 Issue: Volume: Page:
ISSN:1556-5068
Container-title:SSRN Electronic Journal
language:en
Short-container-title:SSRN Journal

Author:

Suuberg Alessandra

Publisher

Elsevier BV

Reference167 articles.

1. Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity;R G Walters;PLoS One,2013

2. Copy number variation in human health, disease, and evolution;F Zhang;Annu Rev Genomics Hum Genet,2015

3. Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes;J R Lupski;PLoS Genet,2005

4. Penetrance for copy number variants associated with schizophrenia;E Vassos;Hum Mol Genet,2010

5. An estimation of the prevalence of genomic disorders using chromosomal microarray data;M A Gillentine;J Hum Genet,2018

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