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Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 10, 2004
FISH analysis helps identify low-level mosaicism in Ullrich-Turner syndrome patientsAnne Wiktor, Daniel L Van DykeCancer Genetics and Cytogenetics|April 18, 2003
Monosomy 21 in hematologic diseasesDaniel L Van Dyke, Anne WiktorCancer Genetics and Cytogenetics|August 25, 2004
Combined cytogenetic testing and fluorescence in situ hybridization analysis in the study of chronic lymphocytic leukemia and multiple myelomaAnne Wiktor, Daniel L Van DykeGenetics in Medicine : Official Journal of the American College of Medical Genetics|January 2, 2003
Diagnostic testing for Prader-Willi syndrome and Angelman syndrome: a cost comparisonKristin G Monaghan, Anne Wiktor, Daniel L Van DykeJournal of the Association of Genetic Technologists|April 15, 2005
Use Reference Bands to Accurately Estimate ISCN Band Levels 400, 550, and 850James Zabawski, Anne Wiktor, Matthew Sikora, et al.American Journal of Medical Genetics. Part A|February 28, 2003
Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delayAlexander Asamoah, Amy B Decker, Anne Wiktor, et al.Cancer Genetics and Cytogenetics|April 7, 2004
Translocation (8;14)(q24;q32) as the sole cytogenetic abnormality in B-cell prolymphocytic leukemiaPhilip Kuriakose, Nusrat Perveen, Koichi Maeda, et al.Genes, Chromosomes & Cancer|June 10, 2004
PRDX4, a member of the peroxiredoxin family, is fused to AML1 (RUNX1) in an acute myeloid leukemia patient with a t(X;21)(p22;q22)Yanming Zhang, Neelmini Emmanuel, Ginny Kamboj, et al.Methods in Molecular Biology (Clifton, N.J.)|October 24, 2018
Analysis of Common Abnormalities Seen in Chronic Lymphocytic Leukemia Using Fluorescence In Situ HybridizationReid G Meyer, Daniel L Van DykeAmerican Journal of Medical Genetics. Part A|September 15, 2005
Detection of low level sex chromosome mosaicism in Ullrich-Turner syndrome patientsAnne E Wiktor, Daniel L Van DykePageof 10