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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.
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.
American Journal of Medical Genetics. Part A|April 6, 2005
Subtelomere deletions and translocations are frequently familialAdewale Adeyinka, S Annie Adams, Cindy P Lorentz, et al.
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