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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 20, 2023
DLG2 intragenic exonic deletions reinforce the link to neurodevelopmental disorders and suggest a potential association with congenital anomalies and dysmorphismYunjia Chen, Ender Karaca, Nathaniel H Robin, et al.
British Journal of Haematology|January 6, 2009
Prevalence and clinical correlates of JAK2 mutations in Down syndrome acute lymphoblastic leukaemiaAmos Gaikwad, Cassia L Rye, Meenakshi Devidas, et al.
American Journal of Medical Genetics. Part A|August 7, 2007
A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR geneFady M Mikhail, Maria Descartes, Arkadiusz Piotrowski, et al.
Blood Advances|October 18, 2021
VpreB surrogate light chain expression in B-lineage ALL: a report from the Children's Oncology GroupStuart S Winter, Amanda McCaustland, Chunxu Qu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2016
Clinical relevance of small copy-number variants in chromosomal microarray clinical testingDana Hollenbeck, Crescenda L Williams, Kathryn Drazba, et al.
Cancer Genetics and Cytogenetics|June 9, 2007
Prognostic significance of cytogenetically detected chromosome 21 anomalies in childhood acute lymphoblastic leukemia: a Pediatric Oncology Group studyLinda D Cooley, Saleen Chenevert, Jonathan J Shuster, et al.
Frontiers in Oncology|March 16, 2026
Case Report: KMT2A amplification in two adult patients with B-cell acute lymphoblastic leukemiaMin Gao, Yunjia Chen, Kimo Bachiashvili, et al.
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