Results 231 to 240 of about 23,382 (272)

Translocation(Y;1)(q12;q12) in hematologic malignancies

Cancer Genetics and Cytogenetics, 1996
Translocation (Y;1)(q12;q12) is a rare cytogenetic anomaly occurring in hematologic disorders thought to affect stem cells. We report here on two new cases, one end-stage myelofibrosis and one chronic myelomonocytic leukemia.
Lucienne Michaux, Iwona Wlodarska, Elvira Rodrigues Pereira Velloso, Gregor Verhoef, Angeline Van Orshoven, Jean-Louis Michaux, Jean-Marie Scheiff, Cristina Mecucci, Herman Van den Berghe   +8 more
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Synovial sarcoma with a secondary chromosome change der(22)t(17;22)(q12;q12)

Cancer Genetics and Cytogenetics, 2002
A consistent, pathognomonic translocation, most commonly a balanced reciprocal translocation, t(X;18) (p11.2;q11.2), is found in more than 90% of synovial sarcomas. We report here a secondary chromosome change, der(22)t(17;22)(q12;q12), in addition to the primary t(X;18)(p11.2;q11.2) in a biphasic synovial sarcoma that occurred in the thigh of a 34 ...
Jun, Nishio, Hiroshi, Iwasaki, Masako, Ishiguro, Yuko, Ohjimi, Teruto, Isayama, Masatoshi, Naito, Yasuhiko, Kaneko, Nanao, Kamada, Masahiro, Kikuchi   +8 more
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del(1)(q12) in adenocarcinomas of the prostate

Cancer Genetics and Cytogenetics, 1996
A structural change of chromosome 1 in q12 may be a new, possibly consistent, chromosome change in adenocarcinoma of the prostate.
H, Qi, P, Dal Cin, W, Van de Voorde, A A, Elgamal, H, Van Poppel, L, Baert, H, Van Den Berghe   +6 more
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Association between der(Y)t(Y;1)(q12;q12) and myelodysplastic syndrome

Cancer Genetics and Cytogenetics, 2001
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Wan, TSK, Ma, SK, Chan, LC, Au, WY
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Interstitial deletion of band q12 of chromosome 5

Clinical Genetics, 1984
A six‐months‐old girl is presented with psychomotor retardation and multiple congenital malformations. The karyotype done on peripheral blood lymphocytes and skin fibroblasts was found to be 46,XX del(5)(411q13). The parents are consanguineous. Their karyotypes were normal.The genes for Arylsulphatase B and Hexosaminidase B are not located in band 5q12.
Deeb, Mary, Dudin, Gertrud, Alexander, Denis, Talj, Fayrouz, Musallam, Salim, Der Kaloustian, Vazken M.   +5 more
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Philadelphia Chromosome with T(6;22) (P25;q12)

New England Journal of Medicine, 1976
The introduction of chromosome analysis in various blood disorders has proved the high specificity of the Philadelphia chromosome — a G22 member with deleted long arms — in the diagnosis of chronic...
Z, Mammon, J, Grinblat, H, Joshua
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A case of lipoblastoma with t(3;8)(q12;q11.2)

Cancer Genetics and Cytogenetics, 1992
We studied a single case of lipoblastoma in a 4-year-old boy. Cytogenetic analysis of the tumor cells showed two abnormal clones: 47,XY,t(3;8)(q12;q11.2),+mar, and 46,XY,t(3;8)(q12;q11.2). To our knowledge, this is the second report of chromosome findings in this rare tumor.
Y, Ohjimi, H, Iwasaki, Y, Kaneko, M, Ishiguro, A, Ohgami, M, Kikuchi   +5 more
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Novel chromosomal translocation (17;22)(q12;q12) in a case of myelodisplastic syndrome characterized with signs of hemolytic anemia at presentation

Gene, 2012
Myelodysplastic syndromes (MDS) are clonal stem cell diseases that can result in cytopenias, dysplasia in one or more cell lineages, infective hematopoiesis, and increase the risk of progression to acute myeloid leukemia (AML). MDSs are characterized by several recurrent cytogenetic defects, which can affect diagnosis, prognosis, and treatment. Some of
Antic D, Impera L, Fekete MD, Djordjevic V, Elezovic I., STORLAZZI, CLELIA TIZIANA   +5 more
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