Rouleau GA - Search Results

1

Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22.

Rouleau GA, Wertelecki W, Haines JL, Hobbs WJ, Trofatter JA, Seizinger BR, Martuza RL, Superneau DW, Conneally PM, Gusella JF. Rouleau GA, et al. Nature. 1987 Sep 17-23;329(6136):246-8. doi: 10.1038/329246a0. Nature. 1987. PMID: 2888021

2

A genetic linkage map of the long arm of human chromosome 22.

Rouleau GA, Haines JL, Bazanowski A, Colella-Crowley A, Trofatter JA, Wexler NS, Conneally PM, Gusella JF. Rouleau GA, et al. Genomics. 1989 Jan;4(1):1-6. doi: 10.1016/0888-7543(89)90306-6. Genomics. 1989. PMID: 2563348

3

Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma.

Seizinger BR, Rouleau GA, Ozelius LJ, Lane AH, Farmer GE, Lamiell JM, Haines J, Yuen JW, Collins D, Majoor-Krakauer D, et al. Seizinger BR, et al. Among authors: rouleau ga. Nature. 1988 Mar 17;332(6161):268-9. doi: 10.1038/332268a0. Nature. 1988. PMID: 2894613

4

Neurofibromatosis 2: clinical and DNA linkage studies of a large kindred.

Wertelecki W, Rouleau GA, Superneau DW, Forehand LW, Williams JP, Haines JL, Gusella JF. Wertelecki W, et al. Among authors: rouleau ga. N Engl J Med. 1988 Aug 4;319(5):278-83. doi: 10.1056/NEJM198808043190505. N Engl J Med. 1988. PMID: 3134615

5

Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis.

Seizinger BR, Rouleau G, Ozelius LJ, Lane AH, St George-Hyslop P, Huson S, Gusella JF, Martuza RL. Seizinger BR, et al. Science. 1987 Apr 17;236(4799):317-9. doi: 10.1126/science.3105060. Science. 1987. PMID: 3105060

6

DNA linkage analysis in Von Recklinghausen neurofibromatosis.

Seizinger BR, Rouleau G, Lane AH, Ozelius LJ, Faryniarz AG, Iannazzi J, Hobbs W, Roy JC, Falcone B, Huson S, et al. Seizinger BR, et al. J Med Genet. 1987 Sep;24(9):529-30. doi: 10.1136/jmg.24.9.529. J Med Genet. 1987. PMID: 3118032 Free PMC article.

7

Models for inherited susceptibility to cancer in the nervous system: a molecular-genetic approach to neurofibromatosis.

Seizinger BR, Martuza RL, Rouleau G, Breakefield XO, Gusella JF. Seizinger BR, et al. Dev Neurosci. 1987;9(3):144-53. doi: 10.1159/000111618. Dev Neurosci. 1987. PMID: 3119309 Review.

8

Molecular genetics of neurofibromatosis 2 and related tumors (acoustic neuroma and meningioma).

Fontaine B, Rouleau GA, Seizinger BR, Menon AG, Jewell AF, Martuza RL, Gusella JF. Fontaine B, et al. Among authors: rouleau ga. Ann N Y Acad Sci. 1991;615:338-43. doi: 10.1111/j.1749-6632.1991.tb37776.x. Ann N Y Acad Sci. 1991. PMID: 2039155 Review.

9

Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.

Rouleau GA, Seizinger BR, Wertelecki W, Haines JL, Superneau DW, Martuza RL, Gusella JF. Rouleau GA, et al. Am J Hum Genet. 1990 Feb;46(2):323-8. Am J Hum Genet. 1990. PMID: 2105641 Free PMC article.

10

Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting.

Fontaine B, Rouleau GA, Seizinger B, Jewell AF, Hanson MP, Martuza RL, Gusella JF. Fontaine B, et al. Among authors: rouleau ga. Am J Hum Genet. 1990 Nov;47(5):823-7. Am J Hum Genet. 1990. PMID: 2220822 Free PMC article.

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