Trisomy 14 in refractory anemia with excess of blasts in transformation
Trisomy 14 was demonstrated on four occasions over a 2-year period in the bone marrow cells of a 63-year-old patient with refractory anemia with excess of blasts in transformation (RAEB-t). Trisomy 14 as the sole karyotype abnormality has been documented in only six malignancies, namely, in two case...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
1987 |
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| Reproduktion: |
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 |
|---|---|
| Übergeordnetes Werk: |
in: Cancer Genetics and Cytogenetics - Amsterdam : Elsevier, 29(1987), 2, Seite 315-318 |
| Übergeordnetes Werk: |
volume:29 ; year:1987 ; number:2 ; pages:315-318 |
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| 520 | |a Trisomy 14 was demonstrated on four occasions over a 2-year period in the bone marrow cells of a 63-year-old patient with refractory anemia with excess of blasts in transformation (RAEB-t). Trisomy 14 as the sole karyotype abnormality has been documented in only six malignancies, namely, in two cases of acute leukemias, one Philadelphia-negative chronic myeloid leukemia, one pancytopenia, and in two colonic polyps. In hematologic neoplasms, this rare primary change preferentially occurs in elderly adults and seems exclusively associated with the myeloid cell lineage. | ||
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(DE-627)NLEJ186658516 (DE-599)GBVNLZ186658516 DE-627 ger DE-627 rakwb eng Trisomy 14 in refractory anemia with excess of blasts in transformation 1987 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Trisomy 14 was demonstrated on four occasions over a 2-year period in the bone marrow cells of a 63-year-old patient with refractory anemia with excess of blasts in transformation (RAEB-t). Trisomy 14 as the sole karyotype abnormality has been documented in only six malignancies, namely, in two cases of acute leukemias, one Philadelphia-negative chronic myeloid leukemia, one pancytopenia, and in two colonic polyps. In hematologic neoplasms, this rare primary change preferentially occurs in elderly adults and seems exclusively associated with the myeloid cell lineage. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Haas, O.A. oth Jager, U. oth Ambros, P. oth Pabinger, I. oth in Cancer Genetics and Cytogenetics Amsterdam : Elsevier 29(1987), 2, Seite 315-318 (DE-627)NLEJ186641591 (DE-600)2004205-X 0165-4608 nnns volume:29 year:1987 number:2 pages:315-318 http://linkinghub.elsevier.com/retrieve/pii/0165-4608(87)90242-1 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 29 1987 2 315-318 |
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(DE-627)NLEJ186658516 (DE-599)GBVNLZ186658516 DE-627 ger DE-627 rakwb eng Trisomy 14 in refractory anemia with excess of blasts in transformation 1987 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Trisomy 14 was demonstrated on four occasions over a 2-year period in the bone marrow cells of a 63-year-old patient with refractory anemia with excess of blasts in transformation (RAEB-t). Trisomy 14 as the sole karyotype abnormality has been documented in only six malignancies, namely, in two cases of acute leukemias, one Philadelphia-negative chronic myeloid leukemia, one pancytopenia, and in two colonic polyps. In hematologic neoplasms, this rare primary change preferentially occurs in elderly adults and seems exclusively associated with the myeloid cell lineage. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Haas, O.A. oth Jager, U. oth Ambros, P. oth Pabinger, I. oth in Cancer Genetics and Cytogenetics Amsterdam : Elsevier 29(1987), 2, Seite 315-318 (DE-627)NLEJ186641591 (DE-600)2004205-X 0165-4608 nnns volume:29 year:1987 number:2 pages:315-318 http://linkinghub.elsevier.com/retrieve/pii/0165-4608(87)90242-1 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 29 1987 2 315-318 |
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(DE-627)NLEJ186658516 (DE-599)GBVNLZ186658516 DE-627 ger DE-627 rakwb eng Trisomy 14 in refractory anemia with excess of blasts in transformation 1987 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Trisomy 14 was demonstrated on four occasions over a 2-year period in the bone marrow cells of a 63-year-old patient with refractory anemia with excess of blasts in transformation (RAEB-t). Trisomy 14 as the sole karyotype abnormality has been documented in only six malignancies, namely, in two cases of acute leukemias, one Philadelphia-negative chronic myeloid leukemia, one pancytopenia, and in two colonic polyps. In hematologic neoplasms, this rare primary change preferentially occurs in elderly adults and seems exclusively associated with the myeloid cell lineage. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Haas, O.A. oth Jager, U. oth Ambros, P. oth Pabinger, I. oth in Cancer Genetics and Cytogenetics Amsterdam : Elsevier 29(1987), 2, Seite 315-318 (DE-627)NLEJ186641591 (DE-600)2004205-X 0165-4608 nnns volume:29 year:1987 number:2 pages:315-318 http://linkinghub.elsevier.com/retrieve/pii/0165-4608(87)90242-1 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 29 1987 2 315-318 |
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(DE-627)NLEJ186658516 (DE-599)GBVNLZ186658516 DE-627 ger DE-627 rakwb eng Trisomy 14 in refractory anemia with excess of blasts in transformation 1987 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Trisomy 14 was demonstrated on four occasions over a 2-year period in the bone marrow cells of a 63-year-old patient with refractory anemia with excess of blasts in transformation (RAEB-t). Trisomy 14 as the sole karyotype abnormality has been documented in only six malignancies, namely, in two cases of acute leukemias, one Philadelphia-negative chronic myeloid leukemia, one pancytopenia, and in two colonic polyps. In hematologic neoplasms, this rare primary change preferentially occurs in elderly adults and seems exclusively associated with the myeloid cell lineage. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Haas, O.A. oth Jager, U. oth Ambros, P. oth Pabinger, I. oth in Cancer Genetics and Cytogenetics Amsterdam : Elsevier 29(1987), 2, Seite 315-318 (DE-627)NLEJ186641591 (DE-600)2004205-X 0165-4608 nnns volume:29 year:1987 number:2 pages:315-318 http://linkinghub.elsevier.com/retrieve/pii/0165-4608(87)90242-1 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 29 1987 2 315-318 |
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(DE-627)NLEJ186658516 (DE-599)GBVNLZ186658516 DE-627 ger DE-627 rakwb eng Trisomy 14 in refractory anemia with excess of blasts in transformation 1987 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Trisomy 14 was demonstrated on four occasions over a 2-year period in the bone marrow cells of a 63-year-old patient with refractory anemia with excess of blasts in transformation (RAEB-t). Trisomy 14 as the sole karyotype abnormality has been documented in only six malignancies, namely, in two cases of acute leukemias, one Philadelphia-negative chronic myeloid leukemia, one pancytopenia, and in two colonic polyps. In hematologic neoplasms, this rare primary change preferentially occurs in elderly adults and seems exclusively associated with the myeloid cell lineage. Elsevier Journal Backfiles on ScienceDirect 1907 - 2002 Haas, O.A. oth Jager, U. oth Ambros, P. oth Pabinger, I. oth in Cancer Genetics and Cytogenetics Amsterdam : Elsevier 29(1987), 2, Seite 315-318 (DE-627)NLEJ186641591 (DE-600)2004205-X 0165-4608 nnns volume:29 year:1987 number:2 pages:315-318 http://linkinghub.elsevier.com/retrieve/pii/0165-4608(87)90242-1 GBV_USEFLAG_H ZDB-1-SDJ GBV_NL_ARTICLE AR 29 1987 2 315-318 |
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trisomy 14 in refractory anemia with excess of blasts in transformation |
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Trisomy 14 in refractory anemia with excess of blasts in transformation |
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Trisomy 14 was demonstrated on four occasions over a 2-year period in the bone marrow cells of a 63-year-old patient with refractory anemia with excess of blasts in transformation (RAEB-t). Trisomy 14 as the sole karyotype abnormality has been documented in only six malignancies, namely, in two cases of acute leukemias, one Philadelphia-negative chronic myeloid leukemia, one pancytopenia, and in two colonic polyps. In hematologic neoplasms, this rare primary change preferentially occurs in elderly adults and seems exclusively associated with the myeloid cell lineage. |
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Trisomy 14 was demonstrated on four occasions over a 2-year period in the bone marrow cells of a 63-year-old patient with refractory anemia with excess of blasts in transformation (RAEB-t). Trisomy 14 as the sole karyotype abnormality has been documented in only six malignancies, namely, in two cases of acute leukemias, one Philadelphia-negative chronic myeloid leukemia, one pancytopenia, and in two colonic polyps. In hematologic neoplasms, this rare primary change preferentially occurs in elderly adults and seems exclusively associated with the myeloid cell lineage. |
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Trisomy 14 was demonstrated on four occasions over a 2-year period in the bone marrow cells of a 63-year-old patient with refractory anemia with excess of blasts in transformation (RAEB-t). Trisomy 14 as the sole karyotype abnormality has been documented in only six malignancies, namely, in two cases of acute leukemias, one Philadelphia-negative chronic myeloid leukemia, one pancytopenia, and in two colonic polyps. In hematologic neoplasms, this rare primary change preferentially occurs in elderly adults and seems exclusively associated with the myeloid cell lineage. |
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