Jonveaux P - Search Results

1

De novo methylation of tumour suppressor genes CDKN2A and CDKN2B is a rare finding in B-cell chronic lymphocytic leukaemia.

Martel V, Guerci A, Humbert JC, Gregoire MJ, Chery M, Lederlin P, Jonveaux P. Martel V, et al. Among authors: jonveaux p. Br J Haematol. 1997 Nov;99(2):320-4. doi: 10.1046/j.1365-2141.1997.3953209.x. Br J Haematol. 1997. PMID: 9375748 Free article.

2

t(14;18) and bcl-2 gene rearrangement in a B-chronic lymphocytic leukaemia.

Jonveaux P, Hillion J, Bennaceur AL, d'Agay MF, Brice P, Daniel MT, Sigaux F, Berger R. Jonveaux P, et al. Br J Haematol. 1992 Aug;81(4):620-1. doi: 10.1111/j.1365-2141.1992.tb03006.x. Br J Haematol. 1992. PMID: 1390255 No abstract available.

3

Mutations of the P53 gene in acute myeloid leukaemia.

Fenaux P, Preudhomme C, Quiquandon I, Jonveaux P, Laï JL, Vanrumbeke M, Loucheux-Lefebvre MH, Bauters F, Berger R, Kerckaert JP. Fenaux P, et al. Among authors: jonveaux p. Br J Haematol. 1992 Feb;80(2):178-83. doi: 10.1111/j.1365-2141.1992.tb08897.x. Br J Haematol. 1992. PMID: 1550773

4

Mutations of the p53 gene in B-cell chronic lymphocytic leukemia: a report on 39 cases with cytogenetic analysis.

Fenaux P, Preudhomme C, Laï JL, Quiquandon I, Jonveaux P, Vanrumbeke M, Sartiaux C, Morel P, Loucheux-Lefebvre MH, Bauters F, et al. Fenaux P, et al. Among authors: jonveaux p. Leukemia. 1992 Apr;6(4):246-50. Leukemia. 1992. PMID: 1588788

5

Leukaemic non-Hodgkin's lymphomas with hyperdiploid cells and t(11;14)(q13;q32): a subtype of mantle cell lymphoma?

Daniel MT, Tigaud I, Flexor MA, Nogueira ME, Berger R, Jonveaux P. Daniel MT, et al. Among authors: jonveaux p. Br J Haematol. 1995 May;90(1):77-84. doi: 10.1111/j.1365-2141.1995.tb03383.x. Br J Haematol. 1995. PMID: 7786799

6

Isochromosome 7q and trisomy 8 are consistent primary, non-random chromosomal abnormalities associated with hepatosplenic T gamma/delta lymphoma.

Jonveaux P, Daniel MT, Martel V, Maarek O, Berger R. Jonveaux P, et al. Leukemia. 1996 Sep;10(9):1453-5. Leukemia. 1996. PMID: 8751461

7

[Familial supravalvular aortic stenosis. Investigation in a family and review of the literature].

Burnel P, Marçon F, Lucron H, Bosser G, Gilgenkrantz S, Jonveaux P, Chéry M, Worms AM. Burnel P, et al. Among authors: jonveaux p. Arch Mal Coeur Vaiss. 1997 May;90(5):719-24. Arch Mal Coeur Vaiss. 1997. PMID: 9295957 Review. French.

8

Characterisation of an inverted X chromosome (p11.2q21.3) associated with mental retardation using FISH.

Sloan-Béna F, Philippe C, LeHeup B, Wuilque F, Levy ER, Chéry M, Jonveaux P, Monaco AP. Sloan-Béna F, et al. Among authors: jonveaux p. J Med Genet. 1998 Feb;35(2):146-50. doi: 10.1136/jmg.35.2.146. J Med Genet. 1998. PMID: 9507395 Free PMC article.

9

The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1.

Popovici C, Zhang B, Grégoire MJ, Jonveaux P, Lafage-Pochitaloff M, Birnbaum D, Pébusque MJ. Popovici C, et al. Among authors: jonveaux p. Blood. 1999 Feb 15;93(4):1381-9. Blood. 1999. PMID: 9949182 Free article.

10

T-cell immune constitution after peripheral blood mononuclear cell transplantation in complete DiGeorge syndrome.

Bensoussan D, Le Deist F, Latger-Cannard V, Grégoire MJ, Avinens O, Feugier P, Bourdon V, André-Botté C, Schmitt C, Jonveaux P, Eliaou JF, Stoltz JF, Bordigoni P. Bensoussan D, et al. Among authors: jonveaux p. Br J Haematol. 2002 Jun;117(4):899-906. doi: 10.1046/j.1365-2141.2002.03496.x. Br J Haematol. 2002. PMID: 12060129 Free article.

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