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Fluorescent in situ hybridization: use of whole chromosome paint probes to identify unbalanced chromosome translocations.
Mayo Clin Proc. 1992 Jul;67(7):658-62. doi: 10.1016/s0025-6196(12)60721-6.
Mayo Clin Proc. 1992.
PMID: 1434900
Fluorescence in situ hybridization: a sensitive method for trisomy 8 detection in bone marrow specimens.
Jenkins RB, Le Beau MM, Kraker WJ, Borell TJ, Stalboerger PG, Davis EM, Penland L, Fernald A, Espinosa R 3rd, Schaid DJ, et al.
Jenkins RB, et al. Among authors: kraker wj.
Blood. 1992 Jun 15;79(12):3307-15.
Blood. 1992.
PMID: 1596571
Free article.
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Use of fluorescent in situ hybridization for marker chromosome identification in congenital and neoplastic disorders.
Schad CR, Kraker WJ, Jalal SM, Tallman MS, Londer HN, Cook LP, Jenkins RB.
Schad CR, et al. Among authors: kraker wj.
Am J Clin Pathol. 1991 Aug;96(2):203-10. doi: 10.1093/ajcp/96.2.203.
Am J Clin Pathol. 1991.
PMID: 1862775
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