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	1641.	Philadelphia-chromosome-positive, monosomy 7 biphenotypic acute mixed lineage leukemia in adults: a pluripotent stem cell disorder. [electronic resource] by Hamaguchi, H Nakamura, Y Nagata, K Shiba, S Arimura, H Muroga, K Miyake, S Ohkawa, Y Morio, T Producer: 19931210 In: Leukemia vol. 7 Availability: No items available. Save to lists Add to cart (remove)
	1642.	Phospholipase D activity is altered in X-linked adrenoleukodystrophy heterozygous carriers, but not in hemizygous patients. [electronic resource] by Logan, H E Byers, D M Ridgway, N D Cook, H W Producer: 19980812 In: Biochimica et biophysica acta vol. 1407 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1643.	Monosomy 6 in human cultured fibroblast-like cells permanently stimulated by fibroblast growth factor 1: evidence for selection. [electronic resource] by Kehrer-Sawatzki, H Röck, H Götz, H Siegel, A Krone, W Producer: 19991027 In: Cytogenetics and cell genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1644.	Characterization of a novel gene, C21orf6, mapping to a critical region of chromosome 21q22.1 involved in the monosomy 21 phenotype and of its murine ortholog, orf5. [electronic resource] by Orti, R Rachidi, M Vialard, F Toyama, K Lopes, C Taudien, S Rosenthal, A Yaspo, M L Sinet, P M Delabar, J M Producer: 20000511 In: Genomics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1645.	Immunosuppressive treatments in Crohn's disease induce myelodysplasia and leukaemia. [electronic resource] by Piccin, Andrea Cortelazzo, Sergio Rovigatti, Ugo Bourke, Billy Smith, Owen P Producer: 20100811 In: American journal of hematology vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1646.	Detection of Turner Syndrome by quantitative PCR of SHOX and VAMP7 genes. [electronic resource] by Ibarra-Ramírez, Marisol Zamudio-Osuna, Michelle Jesús Campos-Acevedo, Luis Daniel Gallardo-Blanco, Hugo Leonid Cerda-Flores, Ricardo Martin Rodríguez-Sánchez, Irám Pablo Martínez-de-Villarreal, Laura Elia Producer: 20151022 In: Genetic testing and molecular biomarkers vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1647.	Mutations of the INI1 rhabdoid tumor suppressor gene in medulloblastomas and primitive neuroectodermal tumors of the central nervous system. [electronic resource] by Biegel, J A Fogelgren, B Zhou, J Y James, C D Janss, A J Allen, J C Zagzag, D Raffel, C Rorke, L B Producer: 20001116 In: Clinical cancer research : an official journal of the American Association for Cancer Research vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	1648.	Extensive cytogenetic studies of clonality following interferon-alpha therapy in chronic myeloid leukemia occurring in monosomic cells in a patient with Turner syndrome mosaic. [electronic resource] by Takeshita, A Shinjo, K Yamashita, M Fujisawa, S Naito, K Ohnishi, K Takahashi, K Matsui, H Ohno, R Producer: 19991207 In: Leukemia vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1649.	Cloning and characterization of a putative human holocytochrome c-type synthetase gene (HCCS) isolated from the critical region for microphthalmia with linear skin defects (MLS). [electronic resource] by Schaefer, L Ballabio, A Zoghbi, H Y Producer: 19970211 In: Genomics vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1650.	Three new cases of chromosome 3 rearrangement in bands q21 and q26 with abnormal thrombopoiesis bring further evidence to the existence of a 3q21q26 syndrome. [electronic resource] by Jotterand Bellomo, M Parlier, V Mühlematter, D Grob, J P Beris, P Producer: 19920612 In: Cancer genetics and cytogenetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1651.	Cytogenetic analysis of myoepithelial cell carcinoma of salivary gland. [electronic resource] by Magrini, Elisabetta Pragliola, Antonella Farnedi, Anna Betts, Christine M Cocchi, Roberto Foschini, Maria P Producer: 20040311 In: Virchows Archiv : an international journal of pathology vol. 444 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1652.	RANBP2-ALK fusion combined with monosomy 7 in acute myelomonocytic leukemia. [electronic resource] by Lim, Ji-Hun Jang, Seongsoo Park, Chan-Jeoung Cho, Young-Uk Lee, Je-Hwan Lee, Kyoo-Hyung Lee, Jin-Ok Shin, Jong-Yeon Kim, Jong-Il Huh, Jooryung Seo, Eul-Ju Producer: 20140512 In: Cancer genetics vol. 207 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1653.	Cytogenetic abnormalities and monosomal karyotypes in children and adolescents with acute myeloid leukemia: correlations with clinical characteristics and outcome. [electronic resource] by Manola, Kalliopi N Panitsas, Fotios Polychronopoulou, Sophia Daraki, Aggeliki Karakosta, Maria Stavropoulou, Cryssa Avgerinou, Georgia Hatzipantelis, Emmanuel Pantelias, Gabriel Sambani, Constantina Pagoni, Maria Producer: 20130531 In: Cancer genetics vol. 206 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1654.	Childhood monosomy 7: epidemiology, biology, and mechanistic implications. [electronic resource] by Luna-Fineman, S Shannon, K M Lange, B J Producer: 19950525 In: Blood vol. 85 Availability: No items available. Save to lists Add to cart (remove)
	1655.	Detection of major and minor bcr/abl fusion gene transcripts in a patient with acute undifferentiated leukemia secondary to treatment with an alkylating agent. [electronic resource] by Hattori, M Tanaka, M Yamazaki, Y Nakahara, Y Tsushita, K Utumi, M Producer: 19950803 In: Leukemia research vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1656.	Genome-wide analysis of subependymomas shows underlying chromosomal copy number changes involving chromosomes 6, 7, 8 and 14 in a proportion of cases. [electronic resource] by Kurian, Kathreena M Jones, David T W Marsden, Faye Openshaw, Sam W S Pearson, Danita M Ichimura, Koichi Collins, V Peter Producer: 20081204 In: Brain pathology (Zurich, Switzerland) vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1657.	Identification of a sugar beet BvM14-MADS box gene through differential gene expression analysis of monosomic addition line M14. [electronic resource] by Ma, Chunquan Wang, Yuguang Wang, Yuting Wang, Lifa Chen, Sixue Li, Haiying Producer: 20130513 In: Journal of plant physiology vol. 168 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1658.	Immunohistochemical characterization of p57Kip2 expression in tetraploid hydropic placentas. [electronic resource] by Fukunaga, Masaharu Producer: 20041214 In: Archives of pathology & laboratory medicine vol. 128 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1659.	Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3. [electronic resource] by Martin, Marcel Maßhöfer, Lars Temming, Petra Rahmann, Sven Metz, Claudia Bornfeld, Norbert van de Nes, Johannes Klein-Hitpass, Ludger Hinnebusch, Alan G Horsthemke, Bernhard Lohmann, Dietmar R Zeschnigk, Michael Producer: 20131017 In: Nature genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1660.	Cytogenetics and comorbidity predict outcomes in older myelodysplastic syndrome patients after allogeneic stem cell transplantation using reduced intensity conditioning. [electronic resource] by Yucel, Orhan Kemal Saliba, Rima M Rondon, Gabriella Ahmed, Sairah Alousi, Amin Bashir, Qaiser Ciurea, Stefan O Popat, Uday Khouri, Isa Marin, David Rezvani, Katy Kebriaei, Partow Shpall, Elizabeth J Champlin, Richard E Oran, Betül Producer: 20170828 In: Cancer vol. 123 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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