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European Journal of Haematology|January 15, 2009
Conventional cytogenetics in myelofibrosis: literature review and discussionKebede Hussein, Daniel L Van Dyke, Ayalew Tefferi
Cancer Genetics|August 8, 2012
When are apparently non-clonal abnormalities in bone marrow chromosome studies actually clonal?Chandra Hutchens, Rhett P Ketterling, Daniel L Van Dyke
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 19, 2010
Laboratory guideline for Turner syndromeDaynna J Wolff, Daniel L Van Dyke, Cynthia M Powell, et al.
American Journal of Medical Genetics. Part A|March 9, 2007
Microarray comparative genomic hybridization and FISH studies of an unbalanced cryptic telomeric 2p deletion/16q duplication in a patient with mental retardation and behavioral problemsYing S Zou, Daniel L Van Dyke, Jay W Ellison
Cancer Genetics|April 17, 2014
Isolated trisomy 2 in bone marrows of patients with suspected hematopoietic malignanciesUmut Aypar, Kaaren K Reichard, Lindsey A Waltman, et al.
Blood Reviews|February 13, 2022
CLL update 2022: A continuing evolution in careNeil E Kay, Paul J Hampel, Daniel L Van Dyke, et al.
American Journal of Medical Genetics. Part A|July 11, 2006
A case of mosaic supernumerary ring chromosome 15 with two copies of the segment 15p11.1-q14Ying S Zou, Pamela S McGrann, Timothy S Uphoff, et al.
Cancer Genetics and Cytogenetics|November 6, 2007
Isochromosome (X)(p10) in hematologic disorders: FISH study of 14 new cases show three types of centromere signal patternsAdewale Adeyinka, Stephanie Smoley, Stephanie Fink, et al.
Blood|November 11, 2009
International Prognostic Scoring System-independent cytogenetic risk categorization in primary myelofibrosisKebede Hussein, Animesh D Pardanani, Daniel L Van Dyke, et al.
American Journal of Medical Genetics. Part A|April 23, 2004
Proximal chromosome 8q deletion in a boy with femoral bifurcation and other multiple congenital anomaliesAlexnder Asamoah, Martin Nwankwo, Savitri P Kumar, et al.
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