Cacheux V - Search Results

1

ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia.

Cavé H, Cacheux V, Raynaud S, Brunie G, Bakkus M, Cochaux P, Preudhomme C, Laï JL, Vilmer E, Grandchamp B. Cavé H, et al. Among authors: cacheux v. Leukemia. 1997 Sep;11(9):1459-64. doi: 10.1038/sj.leu.2400798. Leukemia. 1997. PMID: 9305598

2

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

Raynaud S, Cave H, Baens M, Bastard C, Cacheux V, Grosgeorge J, Guidal-Giroux C, Guo C, Vilmer E, Marynen P, Grandchamp B. Raynaud S, et al. Among authors: cacheux v. Blood. 1996 Apr 1;87(7):2891-9. Blood. 1996. PMID: 8639909 Free article.

3

Localization of the CDKN4/p27Kip1 gene to human chromosome 12p12.3.

Martin E, Cacheux V, Cavé H, Lapierre JM, Le Paslier D, Grandchamp B. Martin E, et al. Among authors: cacheux v. Hum Genet. 1995 Dec;96(6):668-70. doi: 10.1007/BF00210296. Hum Genet. 1995. PMID: 8522324

4

Localization of the human coproporphyrinogen oxidase gene to chromosome band 3q12.

Cacheux V, Martasek P, Fougerousse F, Delfau MH, Druart L, Tachdjian G, Grandchamp B. Cacheux V, et al. Hum Genet. 1994 Nov;94(5):557-9. doi: 10.1007/BF00211026. Hum Genet. 1994. PMID: 7959694

5

Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children.

Gérard B, Le Heuzey MF, Brunie G, Lewine P, Saiag MC, Cacheux V, Da Silva F, Dugas M, Mouren-Simeoni MC, Elion J, Grandchamp B. Gérard B, et al. Among authors: cacheux v. Ann Genet. 1997;40(3):139-44. Ann Genet. 1997. PMID: 9401101 Clinical Trial.

6

Acute lymphoblastic leukemia in the context of RASopathies.

Cavé H, Caye A, Strullu M, Aladjidi N, Vignal C, Ferster A, Méchinaud F, Domenech C, Pierri F, Contet A, Cacheux V, Irving J, Kratz C, Clavel J, Verloes A. Cavé H, et al. Among authors: cacheux v. Eur J Med Genet. 2016 Mar;59(3):173-8. doi: 10.1016/j.ejmg.2016.01.003. Epub 2016 Feb 5. Eur J Med Genet. 2016. PMID: 26855057

7

The MTCP-1/c6.1B gene encodes for a cytoplasmic 8 kD protein overexpressed in T cell leukemia bearing a t(X;14) translocation.

Soulier J, Madani A, Cacheux V, Rosenzwajg M, Sigaux F, Stern MH. Soulier J, et al. Among authors: cacheux v. Oncogene. 1994 Dec;9(12):3565-70. Oncogene. 1994. PMID: 7970717

8

Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.

Lapierre JM, Cacheux V, Collot N, Da Silva F, Hervy N, Rivet D, Romana S, Wiss J, Benzaken B, Aurias A, Tachdjian G. Lapierre JM, et al. Among authors: cacheux v. Ann Genet. 1998;41(3):133-40. Ann Genet. 1998. PMID: 9833066

9

Expression of p13MTCP1 is restricted to mature T-cell proliferations with t(X;14) translocations.

Madani A, Choukroun V, Soulier J, Cacheux V, Claisse JF, Valensi F, Daliphard S, Cazin B, Levy V, Leblond V, Daniel MT, Sigaux F, Stern MH. Madani A, et al. Among authors: cacheux v. Blood. 1996 Mar 1;87(5):1923-7. Blood. 1996. PMID: 8634440 Free article.

10

Prenatal diagnosis of a (X;X) translocation by fluorescence in situ hybridization and laser scanning image cytometry.

Tachdjian G, Cacheux V, Kiefer H, Druart L, Lapierre JM, Oury JF, Blot P, Metezeau P. Tachdjian G, et al. Among authors: cacheux v. Fetal Diagn Ther. 1995 Nov-Dec;10(6):387-92. doi: 10.1159/000264263. Fetal Diagn Ther. 1995. PMID: 8579777

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

69 results

Search Page

Filters