Berger R - Search Results

1

Evidence of chromosomal inversion using fluorescence in situ hybridization to stretched DNA.

Salomon-Nguyen F, Le Coniat-Busson M, Heilig R, Campion D, Weissenbach J, Berger R. Salomon-Nguyen F, et al. Among authors: berger r. C R Acad Sci III. 1998 Jun;321(6):447-52. doi: 10.1016/s0764-4469(98)80775-0. C R Acad Sci III. 1998. PMID: 9769858

2

Fluorescence in situ hybridization analysis of chromosome 1 abnormalities in hematopoietic disorders: rearrangements of DNA satellite II and new recurrent translocations.

Busson-Le Coniat M, Salomon-Nguyen F, Dastugue N, Maarek O, Lafage-Pochitaloff M, Mozziconacci MJ, Baranger L, Brizard F, Radford I, Jeanpierre M, Bernard OA, Berger R. Busson-Le Coniat M, et al. Among authors: berger r. Leukemia. 1999 Dec;13(12):1975-81. doi: 10.1038/sj.leu.2401587. Leukemia. 1999. PMID: 10602418

3

Abnormalities of the short arm of chromosome 12 in T cell prolymphocytic leukemia.

Salomon-Nguyen F, Brizard F, Le Coniat M, Radford I, Berger R, Brizard A. Salomon-Nguyen F, et al. Among authors: berger r. Leukemia. 1998 Jun;12(6):972-5. doi: 10.1038/sj.leu.2401034. Leukemia. 1998. PMID: 9639428

4

MLL-AF1q fusion resulting from t(1;11) in acute leukemia.

Busson-Le Coniat M, Salomon-Nguyen F, Hillion J, Bernard OA, Berger R. Busson-Le Coniat M, et al. Among authors: berger r. Leukemia. 1999 Feb;13(2):302-6. doi: 10.1038/sj.leu.2401299. Leukemia. 1999. PMID: 10025907

5

[A method of molecular hybridization identification of chromosomes purified with a cell sorter].

Bernheim A, Metezeau P, Guellaen G, Weissenbach J, Fellous M, Goldberg M, Berger R. Bernheim A, et al. Among authors: berger r. C R Seances Acad Sci III. 1982 Oct 18;295(6):439-42. C R Seances Acad Sci III. 1982. PMID: 6817878 French. No abstract available.

6

A YAC contig in 6p23 based on sequence tagged sites.

Nemani M, Cherif D, Chesne H, Pelandakis M, Ougen P, Berger R, Weissenbach J, Le Paslier D, Cohen D, Cann HM. Nemani M, et al. Among authors: berger r. Genomics. 1994 Jul 15;22(2):388-96. doi: 10.1006/geno.1994.1400. Genomics. 1994. PMID: 7806226

7

A novel translocation, t(9;11)(q33;q23) involving the HRX gene in an acute monocytic leukemia.

Le Coniat M, Romana SP, Bernard O, Flexor MA, Hillion J, Cherif D, Berger R. Le Coniat M, et al. Among authors: berger r. C R Acad Sci III. 1993 Jul;316(7):692-7. C R Acad Sci III. 1993. PMID: 8019892

8

The t(1;12)(q21;p13) translocation of human acute myeloblastic leukemia results in a TEL-ARNT fusion.

Salomon-Nguyen F, Della-Valle V, Mauchauffe M, Busson-Le Coniat M, Ghysdael J, Berger R, Bernard OA. Salomon-Nguyen F, et al. Among authors: berger r. Proc Natl Acad Sci U S A. 2000 Jun 6;97(12):6757-62. doi: 10.1073/pnas.120162297. Proc Natl Acad Sci U S A. 2000. PMID: 10829078 Free PMC article.

9

A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia.

Bernard OA, Busson-LeConiat M, Ballerini P, Mauchauffé M, Della Valle V, Monni R, Nguyen Khac F, Mercher T, Penard-Lacronique V, Pasturaud P, Gressin L, Heilig R, Daniel MT, Lessard M, Berger R. Bernard OA, et al. Among authors: berger r. Leukemia. 2001 Oct;15(10):1495-504. doi: 10.1038/sj.leu.2402249. Leukemia. 2001. PMID: 11587205

10

Hunting 11q23 deletions with fluorescence in situ hybridization (FISH).

Cherif D, Bernard O, Paulien S, James MR, Le Paslier D, Berger R. Cherif D, et al. Among authors: berger r. Leukemia. 1994 Apr;8(4):578-86. Leukemia. 1994. PMID: 8152254

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