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Refinado por: assunto: Aged remover xxx: xxx remover Oncology remover Genetics & Heredity remover
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1
Multiple cancers in a Turner's syndrome with 45,X/46,XXp - /46,XX/47,XXX karyotype
Multiple cancers in a Turner's syndrome with 45,X/46,XXp - /46,XX/47,XXX karyotype
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Multiple cancers in a Turner's syndrome with 45,X/46,XXp - /46,XX/47,XXX karyotype

Ochi, Hisako ; Takeuchi, Jin ; Sandberg, Avery A.

Cancer genetics and cytogenetics, 1985-04, Vol.16 (4), p.335-339

New York, NY: Elsevier Inc

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2
Malignant solitary fibrous tumor of the soft tissue: a cytogenetic study
Malignant solitary fibrous tumor of the soft tissue: a cytogenetic study
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Malignant solitary fibrous tumor of the soft tissue: a cytogenetic study

Hoshino, Makiko ; Ogose, Akira ; Kawashima, Hiroyuki ; Kudo, Naoko ; Hotta, Tetsuo ; Umezu, Hajime ; Tohyama, Tsuyoshi ; Nakade, Kazuhiro ; Beppu, Hiroki ; Endo, Naoto

Cancer genetics and cytogenetics, 2007-08, Vol.177 (1), p.55-58

United States: Elsevier Inc

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3
Isodicentric (X)(q13): A new characteristic chromosomal anomaly in myeloproliferative syndrome?
Isodicentric (X)(q13): A new characteristic chromosomal anomaly in myeloproliferative syndrome?
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Isodicentric (X)(q13): A new characteristic chromosomal anomaly in myeloproliferative syndrome?

Petit, P. ; Fryns, J.P. ; Masure, R. ; Van Den Berghe, H.

Cancer genetics and cytogenetics, 1982-12, Vol.7 (4), p.339-341

United States: Elsevier Inc

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4
Evidence for the clonal origin of acquired hypomegakaryocytic thrombocytopenic purpura from a sex chromosome mosaic
Evidence for the clonal origin of acquired hypomegakaryocytic thrombocytopenic purpura from a sex chromosome mosaic
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Evidence for the clonal origin of acquired hypomegakaryocytic thrombocytopenic purpura from a sex chromosome mosaic

Nieneltow, Marvin ; Cooper, Milton ; Breg, W.Roy ; Hoffman, Ronald

Cancer genetics and cytogenetics, 1984-01, Vol.12 (3), p.261-265

New York, NY: Elsevier Inc

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5
Genomic aberrations in 80 cases of primary glioblastoma multiforme: Pathogenetic heterogeneity and putative cytogenetic pathways
Genomic aberrations in 80 cases of primary glioblastoma multiforme: Pathogenetic heterogeneity and putative cytogenetic pathways
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Genomic aberrations in 80 cases of primary glioblastoma multiforme: Pathogenetic heterogeneity and putative cytogenetic pathways

Dahlback, Hanne-Sofie S. ; Brandal, Petter ; Meling, Torstein R. ; Gorunova, Ludmila ; Scheie, David ; Heim, Sverre

Genes chromosomes & cancer, 2009-10, Vol.48 (10), p.908-924 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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6
Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93
Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93
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Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93

Mühlbacher, Verena ; Zenger, Melanie ; Schnittger, Susanne ; Weissmann, Sandra ; Kunze, Franziska ; Kohlmann, Alexander ; Bellos, Frauke ; Kern, Wolfgang ; Haferlach, Torsten ; Haferlach, Claudia

Genes chromosomes & cancer, 2014-06, Vol.53 (6), p.524-536 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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7
Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q
Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q
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Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q

Mrózek, Krzysztof ; Heinonen, Kristiina ; Theil, Karl S. ; Bloomfield, Clara D.

Genes chromosomes & cancer, 2002-06, Vol.34 (2), p.137-153 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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8
Insulin-like growth factor binding protein-3 (IGFBP-3) acts as an invasion-metastasis suppressor in ovarian endometrioid carcinoma
Insulin-like growth factor binding protein-3 (IGFBP-3) acts as an invasion-metastasis suppressor in ovarian endometrioid carcinoma
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Insulin-like growth factor binding protein-3 (IGFBP-3) acts as an invasion-metastasis suppressor in ovarian endometrioid carcinoma

TORNG, P.-L ; LEE, Y.-C. G ; HUANG, C.-Y. F ; YE, J.-H ; LIN, Y.-S ; CHU, Y.-W ; HUANG, S.-C ; COHEN, P ; WU, C.-W ; LIN, C.-T

Oncogene, 2008-04, Vol.27 (15), p.2137-2147 [Periódico revisado por pares]

Basingstoke: Nature Publishing

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9
Incidence of 17p deletions and TP53 mutation in myelodysplastic syndrome and acute myeloid leukemia with 5q deletion
Incidence of 17p deletions and TP53 mutation in myelodysplastic syndrome and acute myeloid leukemia with 5q deletion
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Incidence of 17p deletions and TP53 mutation in myelodysplastic syndrome and acute myeloid leukemia with 5q deletion

Sebaa, Amel ; Ades, Lionel ; Baran-Marzack, Fanny ; Mozziconacci, Marie-Joelle ; Penther, Dominique ; Dobbelstein, Sophie ; Stamatoullas, Aspasia ; Récher, Christian ; Prebet, Thomas ; Moulessehoul, Soraya ; Fenaux, Pierre ; Eclache, Virginie

Genes chromosomes & cancer, 2012-12, Vol.51 (12), p.1086-1092 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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10
Common alterations in gene expression and increased proliferation in recurrent acute myeloid leukemia
Common alterations in gene expression and increased proliferation in recurrent acute myeloid leukemia
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Common alterations in gene expression and increased proliferation in recurrent acute myeloid leukemia

STABER, Philipp Bernhard ; LINKESCH, Werner ; ZAUNER, Dorothea ; BEHAM-SCHMID, Christine ; GUELLY, Christian ; SCHAUER, Silvia ; SILL, Heinz ; HOEFLER, Gerald

Oncogene, 2004-01, Vol.23 (4), p.894-904 [Periódico revisado por pares]

Basingstoke: Nature Publishing

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