L. Dietz

Detection of the JAK2 V617F mutation by LightCycler PCR and probe dissociation analysis.

J. Zehnder, Rajan Mariappan, I. Schrijver, 2006, The Journal of molecular diagnostics : JMD.

Identification of an intronic single nucleotide polymorphism leading to allele dropout during validation of a CDH1 sequencing assay: implications for designing polymerase chain reaction-based assays

J. Zehnder, I. Schrijver, N. Chun, 2007, Genetics in Medicine.

Comprehensive and efficient HBB mutation analysis for detection of beta-hemoglobinopathies in a pan-ethnic population.

K. Westover, J. Zehnder, O. Chan, 2010, American journal of clinical pathology.

A multiplex methylation PCR assay for identification of uniparental disomy of chromosome 7

M. Moore, P. Cotter, L. Dietz, 2003, Human mutation.

Prenatal diagnosis of supernumerary marker 15 chromosomes and exclusion of uniparental disomy for chromosome 15

J. Goldberg, P. Cotter, L. Dietz, 1999, Prenatal diagnosis.

Exclusion of maternal uniparental disomy of chromosome 14 in patients referred for Prader-Willi syndrome using a multiplex methylation polymerase chain reaction assay

S. Murphy, R. Jirtle, K. Rauen, 2003, Journal of medical genetics.

Hereditary diffuse gastric cancer due to a previously undescribed CDH1 splice site mutation.

James M Ford, Lisa Dietz, Iris Schrijver, 2010, Human pathology.