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Humangenetik|January 1, 1975
Reproduction in a female patient with Down's syndrome. Case report of a 46, XY child showing slight phenotypical anomalies, born to a 47, XX, + 21 motherS Scharrer, S Stengel-Rutkowski, A Rodewald-Rudescu, et al.Human Genetics|December 1, 1993
Generation of a chromosome-22-specific c-DNA library as confirmed by FISH analysisE Göttert, V Klein, K Piontek, et al.Cancer Genetics and Cytogenetics|September 1, 1993
A further case of acute nonlymphocytic leukemia with tetrasomy 8B Wullich, B Koch, M Schwarz, et al.Genetic Analysis, Techniques and Applications|February 1, 1993
Identification of chromosome-specific sequence-tagged sites by Alu-PCRV Klein, K Piontek, N Brass, et al.The Journal of Pathology|July 1, 1992
A two-colour technique for chromosome in situ hybridization in tissue sectionsS Lutz, C Welter, K D Zang, et al.Der Pathologe|September 24, 2008
[Meningiomas: multiparametric approach for risk stratification and grading]K Yoo-Jin, Y Kim, N Bochem, et al.European Journal of Cancer (Oxford, England : 1990)|January 1, 1994
DNA amplifications on chromosomes 7, 9 and 12 in glioblastoma detected by reverse chromosome paintingU Fischer, B Wullich, H P Sattler, et al.Human Genetics|March 1, 1994
Coamplification on chromosomes 7p12-13 and 9q12-13 identified by reverse chromosome painting in a glioblastoma multiformeU Fischer, B Wullich, H P Sattler, et al.Cytogenetics and Cell Genetics|January 1, 1996
Human endogenous retroviral element k10 (HERV-K10): chromosomal localization by somatic hybrid mapping and fluorescence in situ hybridizationE Meese, E Göttert, K D Zang, et al.Fortschritte Der Neurologie-Psychiatrie|April 12, 2011
[Neurological manifestations of AGel amyloidosis (Meretoja's syndrome) in a German family]J Bürmann, K Fassbender, W Henn, et al.Pageof 14