Aurias A - Search Results

1

Isolation of a novel gene from the DiGeorge syndrome critical region with homology to Drosophila gdl and to human LAMC1 genes.

Demczuk S, Thomas G, Aurias A. Demczuk S, et al. Among authors: aurias a. Hum Mol Genet. 1996 May;5(5):633-8. doi: 10.1093/hmg/5.5.633. Hum Mol Genet. 1996. PMID: 8733130

2

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

3

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

4

Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity.

Demczuk S, Aledo R, Zucman J, Delattre O, Desmaze C, Dauphinot L, Jalbert P, Rouleau GA, Thomas G, Aurias A. Demczuk S, et al. Among authors: aurias a. Hum Mol Genet. 1995 Apr;4(4):551-8. doi: 10.1093/hmg/4.4.551. Hum Mol Genet. 1995. PMID: 7633403

5

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

6

Isolation of a zinc finger gene consistently deleted in DiGeorge syndrome.

Aubry M, Demczuk S, Desmaze C, Aikem M, Aurias A, Julien JP, Rouleau GA. Aubry M, et al. Among authors: aurias a. Hum Mol Genet. 1993 Oct;2(10):1583-7. doi: 10.1093/hmg/2.10.1583. Hum Mol Genet. 1993. PMID: 8268910

7

Isolation of cosmids and fetal brain cDNAs from the proximal long arm of human chromosome 22.

Lamour V, Lévy N, Desmaze C, Baude V, Lécluse Y, Delattre O, Bernheim A, Thomas G, Aurias A, Lipinski M. Lamour V, et al. Among authors: aurias a. Hum Mol Genet. 1993 May;2(5):535-40. doi: 10.1093/hmg/2.5.535. Hum Mol Genet. 1993. PMID: 8518791

8

Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion.

Debrus S, Berger G, de Meeus A, Sauer U, Guillaumont S, Voisin M, Bozio A, Demczuk S, Aurias A, Bouvagnet P. Debrus S, et al. Among authors: aurias a. Hum Genet. 1996 Feb;97(2):138-44. doi: 10.1007/BF02265254. Hum Genet. 1996. PMID: 8566942

9

Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome.

Levy A, Demczuk S, Aurias A, Depétris D, Mattei MG, Philip N. Levy A, et al. Among authors: aurias a. Hum Mol Genet. 1995 Dec;4(12):2417-9. doi: 10.1093/hmg/4.12.2417. Hum Mol Genet. 1995. PMID: 8634722 No abstract available.

10

DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.

Demczuk S, Aurias A. Demczuk S, et al. Among authors: aurias a. Ann Genet. 1995;38(2):59-76. Ann Genet. 1995. PMID: 7486827 Review.

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