Aurias A - Search Results

1

RFLP identified by the anonymous DNA segment FZ V D11 at 22q13 [HGM9 no.D22S80].

Zhang FR, Aurias A, Delattre O, Thomas G. Zhang FR, et al. Among authors: aurias a. Nucleic Acids Res. 1989 Feb 25;17(4):1791. doi: 10.1093/nar/17.4.1791. Nucleic Acids Res. 1989. PMID: 2466241 Free PMC article. No abstract available.

2

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.

3

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.

4

Assessment of chromosome 22 anomalies in neurinomas by combined karyotype and RFLP analyses.

Couturier J, Delattre O, Kujas M, Philippon J, Peter M, Rouleau G, Aurias A, Thomas G. Couturier J, et al. Among authors: aurias a. Cancer Genet Cytogenet. 1990 Mar;45(1):55-62. doi: 10.1016/0165-4608(90)90066-j. Cancer Genet Cytogenet. 1990. PMID: 1967977

5

Mapping of human chromosome 22 with a panel of somatic cell hybrids.

Delattre O, Azambuja CJ, Aurias A, Zucman J, Peter M, Zhang F, Hors-Cayla MC, Rouleau G, Thomas G. Delattre O, et al. Among authors: aurias a. Genomics. 1991 Apr;9(4):721-7. doi: 10.1016/0888-7543(91)90366-m. Genomics. 1991. PMID: 2037296

6

The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus.

Zhang FR, Delattre O, Rouleau G, Couturier J, Lefrançois, Thomas G, Aurias A. Zhang FR, et al. Among authors: aurias a. Genomics. 1990 Jan;6(1):174-7. doi: 10.1016/0888-7543(90)90463-5. Genomics. 1990. PMID: 2303258

7

Mapping of human chromosome 22 by in situ hybridization.

Zhang FR, Aurias A, Delattre O, Stern MH, Benitez J, Rouleau G, Thomas G. Zhang FR, et al. Among authors: aurias a. Genomics. 1990 Jul;7(3):319-24. doi: 10.1016/0888-7543(90)90164-p. Genomics. 1990. PMID: 2365353

8

Recurrent t(11;22) breakpoint mapping by chromosome flow sorting and spot-blot hybridization.

Delattre O, Grunwald M, Bernard A, Grunwald D, Thomas G, Frelat G, Aurias A. Delattre O, et al. Among authors: aurias a. Hum Genet. 1988 Feb;78(2):140-3. doi: 10.1007/BF00278184. Hum Genet. 1988. PMID: 3123358

9

Molecular characterization of ataxia telangiectasia T cell clones. II. The clonal inv(14) in ataxia telangiectasia differs from the inv(14) in T cell lymphoma.

Zhang F, Stern MH, Thomas G, Aurias A. Zhang F, et al. Among authors: aurias a. Hum Genet. 1988 Apr;78(4):316-9. doi: 10.1007/BF00291726. Hum Genet. 1988. PMID: 3258841

10

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

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