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American Journal of Medical Genetics. Part A|June 18, 2009
Molecular cytogenetic characterization of two cases with constitutional distal 11q duplication/triplicationRachel D Burnside, Edward J Lose, Maria G Domínguez, et al.
Disease Models & Mechanisms|June 6, 2015
Variations in dysfunction of sister chromatid cohesion in esco2 mutant zebrafish reflect the phenotypic diversity of Roberts syndromeStefanie M Percival, Holly R Thomas, Adam Amsterdam, et al.
Cytojournal|May 23, 2012
Endoscopic ultrasound and endobronchial ultrasound-guided fine-needle aspiration of deep-seated lymphadenopathy: Analysis of 1338 casesAmberly L Nunez, Nirag C Jhala, Andrew J Carroll, et al.
Human Pathology|December 24, 2003
Osteosarcoma in a patient with McCune-Albright syndrome and Mazabraud's syndrome: a case report emphasizing the cytological and cytogenetic findingsDarshana N Jhala, Isam Eltoum, Andrew J Carroll, et al.
Genes, Chromosomes & Cancer|December 11, 2012
New recurrent balanced translocations in acute myeloid leukemia and myelodysplastic syndromes: cancer and leukemia group B 8461Alison Walker, Krzysztof Mrózek, Jessica Kohlschmidt, et al.
American Journal of Medical Genetics. Part A|November 14, 2008
Distal 22q11.2 microduplication encompassing the BCR geneMaria Descartes, Judy Franklin, Teresita Diaz de Ståhl, et al.
British Journal of Haematology|January 14, 2004
Additional cytogenetic abnormalities in adults with Philadelphia chromosome-positive acute lymphoblastic leukaemia: a study of the Cancer and Leukaemia Group BMeir Wetzler, Richard K Dodge, Krzysztof Mrózek, et al.
Cancer|September 16, 2004
Adult de novo acute myeloid leukemia with t(6;11)(q27;q23): results from Cancer and Leukemia Group B Study 8461 and review of the literatureWilliam Blum, Krzysztof Mrózek, Amy S Ruppert, et al.
American Journal of Medical Genetics. Part A|October 28, 2011
Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disordersFady M Mikhail, Edward J Lose, Nathaniel H Robin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 15, 2013
The recurrent distal 22q11.2 microdeletions are often de novo and do not represent a single clinical entity: a proposed categorization systemFady M Mikhail, Rachel D Burnside, Brooke Rush, et al.
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