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Journal Articles

Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromes

SD Raynaud, M Baens, J Grosgeorge, K Rodgers, CD Reid, M Dainton, M Dyer, JG Fuzibet, N Gratecos, B Taillan, N Ayraud, P Marynen

Blood (1996) 88 (2): 682–689.

https://doi.org/10.1182/blood.V88.2.682.bloodjournal882682

Published: 1996

Journal Articles

The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia

S Raynaud, H Cave, M Baens, C Bastard, V Cacheux, J Grosgeorge, C Guidal-Giroux, C Guo, E Vilmer, P Marynen, B Grandchamp

Blood (1996) 87 (7): 2891–2899.

https://doi.org/10.1182/blood.V87.7.2891.bloodjournal8772891

Published: 1996

Journal Articles

Molecular characterization of 12p abnormalities in hematologic malignancies: deletion of KIP1, rearrangement of TEL, and amplification of CCND2

M Hoglund, B Johansson, J Pedersen-Bjergaard, P Marynen, F Mitelman

Blood (1996) 87 (1): 324–330.

https://doi.org/10.1182/blood.V87.1.324.324

Published: 1996

Journal Articles

TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13)

I Wlodarska, C Mecucci, P Marynen, C Guo, D Franckx, R La Starza, A Aventin, A Bosly, MF Martelli, JJ Cassiman

Blood (1995) 85 (10): 2848–2852.

https://doi.org/10.1182/blood.V85.10.2848.bloodjournal85102848

Published: 1995

Journal Articles

The gene for the alpha 4 subunit of the VLA-4 integrin maps to chromosome 2Q31-32

ZH Zhang, S Vekemans, MS Aly, M Jaspers, P Marynen, JJ Cassiman

Blood (1991) 78 (9): 2396–2399.

https://doi.org/10.1182/blood.V78.9.2396.2396

Published: 1991

NARROW

Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromes

The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia

Molecular characterization of 12p abnormalities in hematologic malignancies: deletion of KIP1, rearrangement of TEL, and amplification of CCND2

TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13)

The gene for the alpha 4 subunit of the VLA-4 integrin maps to chromosome 2Q31-32

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ASH Publications

American Society of Hematology

Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromes

The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia

Molecular characterization of 12p abnormalities in hematologic malignancies: deletion of KIP1, rearrangement of TEL, and amplification of CCND2

TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13)

The gene for the alpha 4 subunit of the VLA-4 integrin maps to chromosome 2Q31-32

Email alerts

ASH Publications

American Society of Hematology

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