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Oncogene|May 15, 1998
An oncogenic fusion product of the phosphatidylinositol 3-kinase p85beta subunit and HUMORF8, a putative deubiquitinating enzymeJ W Janssen, L Schleithoff, C R Bartram, et al.Human Genetics|January 1, 1981
Mutagen-induced sister chromatid exchange rate in Bloom syndrome remains unaltered in the presence of Bloom corrective factorU Schmidt-Preuss, P Maack, C R Bartram, et al.Leukemia|August 1, 1993
SIL-TAL1 deletion in T-cell acute lymphoblastic leukemiaJ W Janssen, W D Ludwig, W Sterry, et al.Oncogene|May 1, 1987
Novel transforming sequences in human acute myelocytic leukemia cell linesJ W Janssen, A C Steenvoorden, M Losekoot, et al.American Journal of Medical Genetics|February 15, 2001
Girl with phenotypic abnormalities and a de novo, apparently balanced translocation 46,XX,t(5;10)(q35.2q11.2)G Zhu, G Gillessen-Kaesbach, J Wirth, et al.Annals of Human Genetics|January 1, 1978
Partial trisomy 13 presumably due to recombination in an inversion heterozygote and by unequal crossing-overT Koske-Westphal, R E Pruszak-Seel, R Niss, et al.Human Molecular Genetics|December 1, 1994
Spectrum of small length germline mutations in the RB1 geneD R Lohmann, B Brandt, W Höpping, et al.Der Pathologe|February 13, 2007
[Enzyme histochemistry of classical and ultrashort Hirschsprung's disease]E Bruder, L M Terracciano, E Passarge, et al.American Journal of Human Genetics|May 1, 1996
The spectrum of RB1 germ-line mutations in hereditary retinoblastomaD R Lohmann, B Brandt, W Höpping, et al.American Journal of Medical Genetics|December 31, 1997
Three brothers with mental and physical retardation, hydrocephalus, microcephaly, internal malformations, speech disorder, and facial anomalies: Mutchinick syndromeW Doerfler, D Wieczorek, G Gillessen-Kaesbach, et al.Pageof 26