Thomas G - Search Results

1

Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas.

Ruttledge MH, Sarrazin J, Rangaratnam S, Phelan CM, Twist E, Merel P, Delattre O, Thomas G, Nordenskjöld M, Collins VP, et al. Ruttledge MH, et al. Among authors: thomas g. Nat Genet. 1994 Feb;6(2):180-4. doi: 10.1038/ng0294-180. Nat Genet. 1994. PMID: 8162072

2

The neurofibromatosis type 2 gene is inactivated in schwannomas.

Twist EC, Ruttledge MH, Rousseau M, Sanson M, Papi L, Merel P, Delattre O, Thomas G, Rouleau GA. Twist EC, et al. Among authors: thomas g. Hum Mol Genet. 1994 Jan;3(1):147-51. doi: 10.1093/hmg/3.1.147. Hum Mol Genet. 1994. PMID: 8162016

3

Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus.

Sanson M, Marineau C, Desmaze C, Lutchman M, Ruttledge M, Baron C, Narod S, Delattre O, Lenoir G, Thomas G, et al. Sanson M, et al. Among authors: thomas g. Hum Mol Genet. 1993 Aug;2(8):1215-20. doi: 10.1093/hmg/2.8.1215. Hum Mol Genet. 1993. PMID: 8401504

4

Analysis of mutations in the SCH gene in schwannomas.

Bijlsma EK, Merel P, Bosch DA, Westerveld A, Delattre O, Thomas G, Hulsebos TJ. Bijlsma EK, et al. Among authors: thomas g. Genes Chromosomes Cancer. 1994 Sep;11(1):7-14. doi: 10.1002/gcc.2870110103. Genes Chromosomes Cancer. 1994. PMID: 7529050

5

Family with neurofibromatosis type 2 and autosomal dominant hearing loss: identification of carriers of the mutated NF2 gene.

Bijlsma EK, Merel P, Fleury P, van Asperen CJ, Westerveld A, Delattre O, Thomas G, Hulsebos TJ. Bijlsma EK, et al. Among authors: thomas g. Hum Genet. 1995 Jul;96(1):1-5. doi: 10.1007/BF00214177. Hum Genet. 1995. PMID: 7607639

6

Analysis of the NF2 tumor-suppressor gene and of chromosome 22 deletions in gliomas.

Hoang-Xuan K, Merel P, Vega F, Hugot JP, Cornu P, Delattre JY, Poisson M, Thomas G, Delattre O. Hoang-Xuan K, et al. Among authors: thomas g. Int J Cancer. 1995 Feb 8;60(4):478-81. doi: 10.1002/ijc.2910600409. Int J Cancer. 1995. PMID: 7829260

7

Dinucleotide repeat polymorphism at the D22S268 locus.

Marineau C, Baron C, Delattre O, Zucman J, Thomas G, Rouleau GA. Marineau C, et al. Among authors: thomas g. Hum Mol Genet. 1993 Mar;2(3):336. doi: 10.1093/hmg/2.3.336-a. Hum Mol Genet. 1993. PMID: 8499931 No abstract available.

8

Physical mapping of the NF2/meningioma region on human chromosome 22q12.

Ruttledge MH, Xie YG, Han FY, Giovannini M, Janson M, Fransson I, Werelius B, Delattre O, Thomas G, Evans G, et al. Ruttledge MH, et al. Among authors: thomas g. Genomics. 1994 Jan 1;19(1):52-9. doi: 10.1006/geno.1994.1012. Genomics. 1994. PMID: 8188242

9

Mapping of the human adenylosuccinate lyase (ADSL) gene to chromosome 22q13.1-->q13.2.

Fon EA, Demczuk S, Delattre O, Thomas G, Rouleau GA. Fon EA, et al. Among authors: thomas g. Cytogenet Cell Genet. 1993;64(3-4):201-3. doi: 10.1159/000133575. Cytogenet Cell Genet. 1993. PMID: 8404037

10

Cloning of six new genes with zinc finger motifs mapping to short and long arms of human acrocentric chromosome 22 (p and q11.2).

Aubry M, Marineau C, Zhang FR, Zahed L, Figlewicz D, Delattre O, Thomas G, de Jong PJ, Julien JP, Rouleau GA. Aubry M, et al. Among authors: thomas g. Genomics. 1992 Jul;13(3):641-8. doi: 10.1016/0888-7543(92)90135-f. Genomics. 1992. PMID: 1639391

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