Showing results (1-10 of 507) with videos related to
Sort By:
Pageof 51
Cytogenetic and Genome Research|March 9, 2004
Multi-locus (ML)-FISH is a reliable tool for nondisjunction studies in human oocytesH Eckel, J Kleinstein, P Wieacker, et al.Human Reproduction (Oxford, England)|July 13, 1999
Frequency of CFTR gene mutations in males participating in an ICSI programmeS Jakubiczka, T Bettecken, M Stumm, et al.Cytogenetic and Genome Research|January 4, 2005
Genotype/phenotype correlation in a patient with partial monosomy 15 and partial trisomy 14M Volleth, M Stumm, J Bürger, et al.Klinische Padiatrie|March 6, 1999
[Trisomy 4p as result of a maternal translocation t(4;8)(q11;p23)]M Stumm, M Reuter, U Mandon, et al.Cancer Genetics and Cytogenetics|May 17, 2000
A novel translocation (17;19)(p13;p13) in a patient with acute myelomonocytic leukemiaR Brückner, K Jentsch-Ullrich, A Franke, et al.Annals of Hematology|March 21, 2002
High reliability and sensitivity of the BCR/ABL1 D-FISH test for the detection of BCR/ABL rearrangementsA F Pelz, H Kröning, A Franke, et al.Cytogenetic and Genome Research|September 7, 2006
Interphase M-FISH applications using commercial probes in prenatal and PGD diagnosticsM Stumm, R-D Wegner, M Bloechle, et al.Human Heredity|October 6, 2001
Preferential inactivation of a dupX(q23 --> q27-28) chromosome in a girl with mental retardation and dysmorphyM Volleth, M Stumm, K Mohnike, et al.Cytogenetics and Cell Genetics|July 4, 2001
High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndromeM Stumm, S Neubauer, S Keindorff, et al.Cytogenetics and Cell Genetics|February 15, 2001
Female pseudohermaphroditism caused by caudal dysgenesisP Wieacker, U Grumpelt, T Schulz, et al.Pageof 51