PMID- 9283600 OWN - NLM STAT- MEDLINE DCOM- 19970917 LR - 20190816 IS - 0165-4608 (Print) IS - 0165-4608 (Linking) VI - 97 IP - 2 DP - 1997 Sep TI - Identification of pericentric inversion 12, inv(12)(p13.1q11), by fluorescence in situ hybridization in a patient with acute myeloid leukemia (AML-M6). PG - 157-60 AB - Using probes located between 12p12.1 and 12p13.3, we performed fluorescence in situ hybridization (FISH) analysis and identified an inv(12)(p13.1q11) in a patient with acute myeloid leukemia (AML-M6). Standard cytogenetic analysis had identified the rearranged chromosomes 12 as del(12) (p11p13). Although deletions and translocations involving band 12p13 are fairly common chromosomal abnormalities observed in a broad spectrum of hematologic malignancies, inv(12) is a rather rare abnormality. We compare the clinical and cytogenetic findings with those of the previous cases reported in the literature. FAU - Sato, Y AU - Sato Y AD - Section of Hematology/Oncology, University of Chicago, IL 60637, USA. FAU - Bohlander, S K AU - Bohlander SK FAU - Kobayashi, H AU - Kobayashi H FAU - Suto, Y AU - Suto Y FAU - Davis, E M AU - Davis EM FAU - Espinosa, R 3rd AU - Espinosa R 3rd FAU - Le Beau, M M AU - Le Beau MM FAU - Rowley, J D AU - Rowley JD LA - eng GR - CA40046/CA/NCI NIH HHS/United States GR - CA42557/CA/NCI NIH HHS/United States PT - Case Reports PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, Non-P.H.S. PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - Cancer Genet Cytogenet JT - Cancer genetics and cytogenetics JID - 7909240 RN - 0 (DNA Probes) SB - IM MH - Chromosome Banding MH - *Chromosome Inversion MH - Chromosome Mapping MH - *Chromosomes, Human, Pair 12 MH - DNA Probes MH - Female MH - Humans MH - In Situ Hybridization, Fluorescence MH - Karyotyping MH - Leukemia, Erythroblastic, Acute/*genetics MH - Middle Aged EDAT- 1997/09/01 00:00 MHDA- 2001/03/28 10:01 CRDT- 1997/09/01 00:00 PHST- 1997/09/01 00:00 [pubmed] PHST- 2001/03/28 10:01 [medline] PHST- 1997/09/01 00:00 [entrez] AID - S0165460896003354 [pii] AID - 10.1016/s0165-4608(96)00335-4 [doi] PST - ppublish SO - Cancer Genet Cytogenet. 1997 Sep;97(2):157-60. doi: 10.1016/s0165-4608(96)00335-4.