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- [1] Partial trisomy 18q11.2→qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization ANNALES DE GENETIQUE, 2004, 47 (04): : 393 - 398
- [2] Fluorescence in situ hybridization analysis in a case of de novo unbalanced translocation CYTOGENETICS AND CELL GENETICS, 1999, 85 (1-2): : 158 - 158
- [5] Characterization of a de novo unbalanced chromosome rearrangement by comparative genomic hybridization and fluorescence in situ hybridization CYTOGENETICS AND CELL GENETICS, 1997, 76 (1-2): : 68 - 71
- [6] UNBALANCED TRANSLOCATION, T(18 21), DETECTED BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) IN A CHILD WITH 18Q-SYNDROME AND A RING CHROMOSOME-21 AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 46 (06): : 647 - 651
- [7] Detection of translocation t(11;14)(q13;q32) in mantle cell lymphoma by fluorescence in situ hybridization AMERICAN JOURNAL OF PATHOLOGY, 1999, 154 (05): : 1449 - 1452
- [8] Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation T(18p;21Q) by fluorescence in situ hybridisation GENETIC COUNSELING, 2002, 13 (02): : 151 - 156