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Cancer Genetics and Cytogenetics|August 1, 1995
Chromosome aberrations, spontaneous SCE, and growth kinetics in PHA-stimulated lymphocytes of five cases with Sézary syndromeJ Limon, B Nedoszytko, I Brozek, et al.Klinika Oczna|August 1, 1994
[VNTR-PCR in diagnosis of inherited Rb gene mutation]S Zajaczek, B Górski, T Débniak, et al.Journal of Human Genetics|October 6, 2001
The DIRC1 gene at chromosome 2q33 spans a familial RCC-associated t(2;3)(q33;q21) chromosome translocationT Druck, J Podolski, T Byrski, et al.Cancer Genetics and Cytogenetics|March 12, 1998
Translocation (X;1)(p11.2;q21) in a papillary renal cell carcinoma in a 14-year-old girlI Kardaś, A Denis, M Babińska, et al.Journal of Human Genetics|January 5, 2002
Characterization of a familial RCC-associated t(2;3)(q33;q21) chromosome translocationJ Podolski, T Byrski, S Zajaczek, et al.Acta Geneticae Medicae Et Gemellologiae|August 1, 2000
Prevalence and forms of congenital anomalies in twins born in Pomeranian District during the period from 1.07.1997 to 31.12.1998. Polish Register of Congenital AnomaliesT Zimoń, M Walczak, J Fydryk, et al.Pageof 2