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Found 3 results

2009
Miller ND, Nance MA, Wohler ES, Hoover-Fong JE, Lisi E, Thomas GH, Pevsner J.  2009.  Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function.. American journal of medical genetics. Part A. 149A(4):669-80. Abstract
2008
Wang W, Carvalho B, Miller ND, Pevsner J, Chakravarti A, Irizarry RA.  2008.  Estimating genome-wide copy number using allele-specific mixture models.. Journal of computational biology : a journal of computational molecular cell biology. 15(7):857-66. Abstract
2007
Ting JC, Roberson EDO, Miller ND, Lysholm-Bernacchi A, Stephan DA, Capone GT, Ruczinski I, Thomas GH, Pevsner J.  2007.  Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio.. Human mutation. 28(12):1225-35. Abstract

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