Aurias A - Search Results

1

The RB1 gene is the target of chromosome 13 deletions in malignant fibrous histiocytoma.

Chibon F, Mairal A, Fréneaux P, Terrier P, Coindre JM, Sastre X, Aurias A. Chibon F, et al. Among authors: aurias a. Cancer Res. 2000 Nov 15;60(22):6339-45. Cancer Res. 2000. PMID: 11103795

2

Fluorescence in situ hybridization determination of 22q12-q13 deletion in two intracerebral ependymomas.

Rousseau-Merck M, Versteege I, Zattara-Cannoni H, Figarella D, Lena G, Aurias A, Vagner-Capodano AM. Rousseau-Merck M, et al. Among authors: aurias a. Cancer Genet Cytogenet. 2000 Sep;121(2):223-7. doi: 10.1016/s0165-4608(00)00262-4. Cancer Genet Cytogenet. 2000. PMID: 11063814

3

Molecular analysis of chromosome arm 17q gain in neuroblastoma.

Janoueix-Lerosey I, Penther D, Thioux M, de Crémoux P, Derré J, Ambros P, Vielh P, Bénard J, Aurias A, Delattre O. Janoueix-Lerosey I, et al. Among authors: aurias a. Genes Chromosomes Cancer. 2000 Jul;28(3):276-84. doi: 10.1002/1098-2264(200007)28:3<276::aid-gcc5>3.0.co;2-p. Genes Chromosomes Cancer. 2000. PMID: 10862033

4

Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization.

Demczuk S, Desmaze C, Aikem M, Prieur M, Ledeist F, Sanson M, Rouleau G, Thomas G, Aurias A. Demczuk S, et al. Among authors: aurias a. Ann Genet. 1994;37(2):60-5. Ann Genet. 1994. PMID: 7985979

5

Physical mapping of 30 CA repeats on human chromosome 22.

Demczuk S, Delattre O, Vignal A, Weissenbach J, Thomas G, Aurias A. Demczuk S, et al. Among authors: aurias a. Genomics. 1995 May 20;27(2):345-7. doi: 10.1006/geno.1995.1053. Genomics. 1995. PMID: 7558003

6

Molecular characterization of different ataxia telangiectasia T-cell clones. I. A common breakpoint at the 14q11.2 band splits the T-cell receptor alpha-chain gene.

Stern MH, Zhang FR, Griscelli C, Thomas G, Aurias A. Stern MH, et al. Among authors: aurias a. Hum Genet. 1988 Jan;78(1):33-6. doi: 10.1007/BF00291230. Hum Genet. 1988. PMID: 3422210

7

Molecular characterization of ataxia telangiectasia T cell clones. III. Mapping the 14q32.1 distal breakpoint.

Stern MH, Zhang FR, Thomas G, Griscelli C, Aurias A. Stern MH, et al. Among authors: aurias a. Hum Genet. 1988 Dec;81(1):18-22. doi: 10.1007/BF00283722. Hum Genet. 1988. PMID: 3264259

8

RFLP identified by the anonymous DNA segment FZ VI A2 at 22q11.2 [HGM no. D22S20].

Zhang FR, Monpezat JP, Delattre O, Aurias A, Thomas G. Zhang FR, et al. Among authors: aurias a. Nucleic Acids Res. 1988 Mar 25;16(6):2739. doi: 10.1093/nar/16.6.2739. Nucleic Acids Res. 1988. PMID: 2896336 Free PMC article. No abstract available.

9

RFLP identified by the anonymous DNA segment FZ IV E11 at 1p23 [HGM9 no.D1S87].

Zhang FG, Aurias A, de Taud MF, Gross MS, N'guyen VC, Thomas G. Zhang FG, et al. Among authors: aurias a. Nucleic Acids Res. 1989 Feb 25;17(4):1788. doi: 10.1093/nar/17.4.1788. Nucleic Acids Res. 1989. PMID: 2564194 Free PMC article. No abstract available.

10

Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome).

Zhang F, Deleuze JF, Aurias A, Dutrillaux AM, Hugon RN, Alagille D, Thomas G, Hadchouel M. Zhang F, et al. Among authors: aurias a. J Pediatr. 1990 Jan;116(1):73-7. doi: 10.1016/s0022-3476(05)81648-8. J Pediatr. 1990. PMID: 1967307

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