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What are the appropriate molecular cytogenetic approaches that should be used to diagnose the following cases? Why? Please explain. 1. Phenotypically abnormal child with balanced 46,XX,t(7;8)(q12;p22) karyotype. 2. A cancer case with a complex translocation that detected by karyotyping, but origins of involved chromosomes was not identified. 3. A balanced translocation carrier woman with recurrent abortions planning a new pregnancy. 4. Bronchial lavage material taken on suspicion of lung cancer 5. A case suspected of having terminal deletion in the short arm of chromosome 5.
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