Publications by authors named "Heidi Whitby"

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An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Erin B Kaminsky, Vineith Kaul, Justin Paschall, Deanna M Church, Brian Bunke, Heidi Whitby

Genet Med· September 2011

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Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype.
Sarah T South, Heidi Whitby, Teresa Maxwell, Emily Aston, Arthur R Brothman

Am J Med Genet A· October 2008

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Homozygous deletions of a copy number change detected by array CGH: a new cause for mental retardation?
Cynthia J Curry, Rong Mao, Emily Aston, Shella K Mongia, Tamara Treisman, Heidi Whitby

Am J Med Genet A· August 2008

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Comprehensive analysis of Wolf-Hirschhorn syndrome using array CGH indicates a high prevalence of translocations.
Sarah T South, Heidi Whitby, Agatino Battaglia, John C Carey, Arthur R Brothman

Eur J Hum Genet· January 2008

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Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardation.
Annika M Svensson, Cynthia J Curry, Sarah T South, Heidi Whitby, Teresa M Maxwell

Am J Med Genet A· June 2007

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