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The Journal of Molecular Diagnostics : JMD|March 20, 2012
Parent-of-origin testing for 15q11-q13 gains by quantitative DNA methylation analysisS Hussain Askree, Shika Dharamrup, Lawrence N Hjelm, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Characterization of an unusual deletion of the galactose-1-phosphate uridyl transferase (GALT) geneBradford Coffee, Lawrence N Hjelm, Angela DeLorenzo, et al.
American Journal of Medical Genetics. Part A|April 17, 2008
Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: a case report and review of the literatureBradford Coffee, Morna Ikeda, Dejan B Budimirovic, et al.
The Journal of Molecular Diagnostics : JMD|July 20, 2010
A simple method to confirm and size deletion, duplication, and insertion mutations detected by sequence analysisLawrence N Hjelm, Ephrem L H Chin, Madhuri R Hegde, et al.
The Journal of Molecular Diagnostics : JMD|January 14, 2011
Allelic dropout can cause false-positive results for Prader-Willi and Angelman syndrome testingSyed Hussain Askree, Lawrence N Hjelm, Muhammad Ali Pervaiz, et al.
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