Publications by authors named "Cameron Mroske"

14Publications

CLTC as a clinically novel gene associated with multiple malformations and developmental delay.

Am J Med Genet A 2016 Apr 29;170A(4):958-66. Epub 2016 Jan 29.

Department of Pediatrics, Section of Medical Genetics, SUNY Upstate Medical University, Syracuse, New York.

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April 2016

Diagnostic exome sequencing provides a molecular diagnosis for a significant proportion of patients with epilepsy.

Genet Med 2016 09 21;18(9):898-905. Epub 2016 Jan 21.

Division of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

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September 2016

A capillary electrophoresis sequencing method for the identification of mutations in the inverted terminal repeats of adeno-associated virus.

Hum Gene Ther Methods 2012 Apr 21;23(2):128-36. Epub 2012 May 21.

Division of Hematology and Division of Stem Cell Transplantation, City of Hope, Duarte, CA 91010, USA.

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April 2012

Toward a fluorescent single-strand conformation polymorphism technique that detects all mutations: F-DOVAM-S.

Anal Biochem 2007 Sep 26;368(2):250-7. Epub 2007 May 26.

Department of Molecular Genetics and Department of Molecular Diagnosis, City of Hope National Medical Center, Duarte, CA 91010, USA.

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September 2007

TNF ligands: is TALL-1 a trimer or a virus-like cluster?

Nature 2004 Jan;427(6973):413-4; discussion 414

Xencor, Monrovia, California 91016, USA.

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January 2004

A fluorescence microscopy method for quantifying levels of prostaglandin endoperoxide H synthase-1 and CD-41 in MEG-01 cells.

Biol Proced Online 2001 Dec;3:54-63

Department of Pathology and Laboratory Medicine, Faculty of Medicine, University of Ottawa. 451 Smyth Road, Ottawa, K1H 8M5. Canada. ext. 8330; Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa. Canada.

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December 2001