A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33

Ryan N. Traylor; Damien L. Bruno; Trent Burgess; Robert Wildin; Anne Spencer; Devika Ganesamoorthy; David J. Amor; Matthew Hunter; Michael Caplan; Jill A. Rosenfeld; Aaron Theisen; Beth S. Torchia; Lisa G. Shaffer; Blake C. Ballif; Howard R. Slater

doi:10.1371/journal.pone.0012462

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Open Access

Peer-reviewed

Research Article

A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33

Ryan N. Traylor,

Affiliation Signature Genomic Laboratories, Spokane, Washington, United States of America
⨯
Damien L. Bruno,

Affiliations Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia, Department of Pediatrics, University of Melbourne, Royal Children's Hospital, Parkville, Victoria, Australia
⨯
Trent Burgess,

Affiliations Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia, Department of Pediatrics, University of Melbourne, Royal Children's Hospital, Parkville, Victoria, Australia
⨯
Robert Wildin,

Affiliation St. Luke's Regional Medical Center, Boise, Idaho, United States of America
⨯
Anne Spencer,

Affiliation St. Luke's Regional Medical Center, Boise, Idaho, United States of America
⨯
Devika Ganesamoorthy,

Affiliations Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia, Department of Pediatrics, University of Melbourne, Royal Children's Hospital, Parkville, Victoria, Australia
⨯
David J. Amor,

Affiliations Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia, Department of Pediatrics, University of Melbourne, Royal Children's Hospital, Parkville, Victoria, Australia
⨯
Matthew Hunter,

Affiliation Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia
⨯
Michael Caplan,

Affiliation Northshore University Healthsystem, Pritzker School of Medicine, University of Chicago, Chicago, Illinois, United States of America
⨯
Jill A. Rosenfeld,

Affiliation Signature Genomic Laboratories, Spokane, Washington, United States of America
⨯
Aaron Theisen,

Affiliation Signature Genomic Laboratories, Spokane, Washington, United States of America
⨯
Beth S. Torchia,

Affiliation Signature Genomic Laboratories, Spokane, Washington, United States of America
⨯
Lisa G. Shaffer,

Affiliation Signature Genomic Laboratories, Spokane, Washington, United States of America
⨯
Blake C. Ballif ,

* E-mail: ballif@signaturegenomics.com

Affiliation Signature Genomic Laboratories, Spokane, Washington, United States of America
⨯
Howard R. Slater

Affiliations Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia, Department of Pediatrics, University of Melbourne, Royal Children's Hospital, Parkville, Victoria, Australia
⨯

A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33

Ryan N. Traylor,
Damien L. Bruno,
Trent Burgess,
Robert Wildin,
Anne Spencer,
Devika Ganesamoorthy,
David J. Amor,
Matthew Hunter,
Michael Caplan,
Jill A. Rosenfeld

Published: August 27, 2010
https://doi.org/10.1371/journal.pone.0012462

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