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Results:
1-19
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Results: 19
Authors:
Soulier, J
Pierron, G
Vecchione, D
Garand, R
Brizard, F
Sigaux, F
Stern, MH
Aurias, A
Citation: J. Soulier et al., A complex pattern of recurrent chromosomal bosses and gains in T-cell prolymphocytic leukemia, GENE CHROM, 31(3), 2001, pp. 248-254
Authors:
Gad, S
Aurias, A
Puget, N
Mairal, A
Schurra, C
Montagna, M
Pages, S
Caux, V
Mazoyer, S
Bensimon, A
Stoppa-Lyonnet, D
Citation: S. Gad et al., Color bar coding the BRCAI gene on combed DNA: A useful strategy for detecting large gene rearrangements, GENE CHROM, 31(1), 2001, pp. 75-84
Authors:
Gad, S
Stoppa-Lyonnet, D
Aurias, A
Bensimon, A
Citation: S. Gad et al., Colour bar coding on combed DNA revealed large gene rearrangements of BRCA1 gene, M S-MED SCI, 17(10), 2001, pp. 1072-1075
Authors:
Brisset, S
Schleiermacher, G
Peter, M
Mairal, A
Oberlin, O
Delattre, O
Aurias, A
Citation: S. Brisset et al., CGH analysis of secondary genetic changes in Ewing tumors: correlation with metastatic disease in a series of 43 cases, CANC GENET, 130(1), 2001, pp. 57-61
Authors:
Derre, J
Lagace, R
Terrier, P
Sastre, X
Aurias, A
Citation: J. Derre et al., Consistent DNA losses on the short arm of chromosome 1 in a series of malignant gastrointestinal stromal tumors, CANC GENET, 127(1), 2001, pp. 30-33
Authors:
Derre, J
Lagace, R
Nicolas, A
Mairal, A
Chibon, F
Coindre, JM
Terrier, P
Sastre, X
Aurias, A
Citation: J. Derre et al., Leiomyosarcomas and most malignant fibrous histiocytomas share very similar comparative genomic hybridization imbalances: An analysis of a series of 27 leiomyosarcomas, LAB INV, 81(2), 2001, pp. 211-215
Authors:
Gad, S
Scheuner, MT
Pages-Berhouet, S
Caux-Moncoutier, V
Bensimon, A
Aurias, A
Pinto, M
Stoppa-Lyonnet, D
Citation: S. Gad et al., Identification of a large rearrangement of the BRCA1 gene using colour barcode on combed DNA in an American breast/ovarian cancer family previously studied by direct sequencing, J MED GENET, 38(6), 2001, pp. 388-392
Authors:
Geoffroy-Perez, B
Janin, N
Ossian, K
Lauge, A
Croquette, MF
Griscelli, C
Debre, M
Bressac-De-Paillerets, B
Aurias, A
Stoppa-Lyonnet, D
Andrieu, N
Citation: B. Geoffroy-perez et al., Cancer risk in heterozygotes for ataxia-telangiectasia, INT J CANC, 93(2), 2001, pp. 288-293
Authors:
Joly, G
Lapierre, JM
Ozilou, C
Gosset, P
Aurias, A
de Blois, MC
Prieur, M
Raoul, O
Colleaux, L
Munnich, A
Romana, SP
Vekemans, M
Turleau, C
Citation: G. Joly et al., Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype, CLIN GENET, 60(3), 2001, pp. 212-219
Authors:
Mairal, A
Pinglier, E
Gilbert, E
Peter, M
Validire, P
Desjardins, L
Doz, F
Aurias, A
Couturier, J
Citation: A. Mairal et al., Detection of chromosome imbalances in retinoblastoma by parallel karyotypeand CGH analyses, GENE CHROM, 28(4), 2000, pp. 370-379
Authors:
Janoueix-Lerosey, I
Penther, D
Thioux, M
de Cremoux, P
Derre, J
Ambros, P
Vielh, P
Benard, J
Aurias, A
Delattre, O
Citation: I. Janoueix-lerosey et al., Molecular analysis of chromosome arm 17q gain neuroblastoma, GENE CHROM, 28(3), 2000, pp. 276-284
Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study
Authors:
Lapierre, JM
Cacheux, V
Luton, D
Collot, N
Oury, JF
Aurias, A
Tachdjian, G
Citation: Jm. Lapierre et al., Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study, PRENAT DIAG, 20(2), 2000, pp. 123-131
Authors:
Mairal, A
Chibon, F
Rousselet, A
Couturier, J
Terrier, P
Aurias, A
Citation: A. Mairal et al., Establishment of a human malignant fibrous histiocytoma cell line, COMA: Characterization by conventional cytogenetics, comparative genomic hybridization, and multiplex fluorescence in situ hybridization, CANC GENET, 121(2), 2000, pp. 117-123
Authors:
Rousseau-Merck, MF
Versteege, I
Zattara-Cannoni, H
Figarella, D
Lena, G
Aurias, A
Vagner-Capodano, AM
Citation: Mf. Rousseau-merck et al., Fluorescence in situ hybridization determination of 22q12-q13 deletion in two intracerebral ependymomas, CANC GENET, 121(2), 2000, pp. 223-227
Authors:
Chibon, F
Mairal, A
Freneaux, P
Terrier, P
Coindre, JM
Sastre, X
Aurias, A
Citation: F. Chibon et al., The RB1 gene is the target of chromosome 13 deletions in malignant fibroushistiocytoma, CANCER RES, 60(22), 2000, pp. 6339-6345
Authors:
Mairal, A
Terrier, P
Chibon, F
Sastre, X
Lecesne, A
Aurias, A
Citation: A. Mairal et al., Loss of chromosome 13 is the most frequent genomic imbalance in malignant fibrous histiocytomas - A comparative genomic hybridization analysis of a series of 30 cases, CANC GENET, 111(2), 1999, pp. 134-138
Authors:
Rousseau-Merck, MF
Versteege, I
Legrand, I
Couturier, J
Mairal, A
Delattre, O
Aurias, A
Citation: Mf. Rousseau-merck et al., hSNF5/INI1 inactivation is mainly associated with homozygous deletions andmitotic recombinations in rhabdoid tumors, CANCER RES, 59(13), 1999, pp. 3152-3156
Authors:
Soussi, T
Aurias, A
Giovannini, M
Zucman-Rossi, J
Citation: T. Soussi et al., Neurofibromatosis type-2 (Tumor suppressor gene), B CANCER, 86(12), 1999, pp. 963-964
Authors:
Janin, N
Andrieu, N
Ossian, K
Lauge, A
Croquette, MF
Griscelli, C
Debre, M
Bressac-de-Paillerets, B
Aurias, A
Stoppa-Lyonnet, D
Citation: N. Janin et al., Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families, BR J CANC, 80(7), 1999, pp. 1042-1045
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