Fontaine B - Search Results

1

Loss of chromosome 22 alleles in human sporadic spinal schwannomas.

Fontaine B, Hanson MP, VonSattel JP, Martuza RL, Gusella JF. Fontaine B, et al. Ann Neurol. 1991 Feb;29(2):183-6. doi: 10.1002/ana.410290211. Ann Neurol. 1991. PMID: 2012386

2

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. 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.

3

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. Am J Hum Genet. 1990 Nov;47(5):823-7. Am J Hum Genet. 1990. PMID: 2220822 Free PMC article.

4

Parental origin of chromosome 22 loss in sporadic and NF2 neuromas.

Fontaine B, Sanson M, Delattre O, Menon AG, Rouleau GA, Seizinger BR, Jewell AF, Hanson MP, Aurias A, Martuza RL, et al. Fontaine B, et al. Genomics. 1991 May;10(1):280-3. doi: 10.1016/0888-7543(91)90513-e. Genomics. 1991. PMID: 1675196

5

The alpha-subunit of the skeletal muscle sodium channel is encoded proximal to Tk-1 on mouse chromosome 11.

Ambrose C, Cheng S, Fontaine B, Nadeau JH, MacDonald M, Gusella JF. Ambrose C, et al. Among authors: fontaine b. Mamm Genome. 1992;3(3):151-5. doi: 10.1007/BF00352459. Mamm Genome. 1992. PMID: 1352160

6

BanI polymorphism at the XBP1 locus.

Fontaine B, Hanson MP, Liou HC, Glimcher LH, Rouleau GA, Gusella JF. Fontaine B, et al. Nucleic Acids Res. 1990 Sep 25;18(18):5578. doi: 10.1093/nar/18.18.5578-a. Nucleic Acids Res. 1990. PMID: 1977120 Free PMC article.

7

Different gene loci for hyperkalemic and hypokalemic periodic paralysis.

Fontaine B, Trofatter J, Rouleau GA, Khurana TS, Haines J, Brown R, Gusella JF. Fontaine B, et al. Neuromuscul Disord. 1991;1(4):235-8. doi: 10.1016/0960-8966(91)90095-a. Neuromuscul Disord. 1991. PMID: 1822800

8

Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene.

Fontaine B, Khurana TS, Hoffman EP, Bruns GA, Haines JL, Trofatter JA, Hanson MP, Rich J, McFarlane H, Yasek DM, et al. Fontaine B, et al. Science. 1990 Nov 16;250(4983):1000-2. doi: 10.1126/science.2173143. Science. 1990. PMID: 2173143

9

A set of STS assays targeting the chromosome 22 physical framework markers.

MacCollin M, Romano D, Budarf M, Denny C, Trofatter J, Menon A, Rouleau G, Fontaine B, Emanuel B, Gusella J. MacCollin M, et al. Among authors: fontaine b. Genomics. 1993 Mar;15(3):680-3. doi: 10.1006/geno.1993.1125. Genomics. 1993. PMID: 8468063

10

Juvenile-onset spinal muscular atrophy caused by compound heterozygosity for mutations in the HEXA gene.

Navon R, Khosravi R, Melki J, Drucker L, Fontaine B, Turpin JC, N'Guyen B, Fardeau M, Rondot P, Baumann N. Navon R, et al. Among authors: fontaine b. Ann Neurol. 1997 May;41(5):631-8. doi: 10.1002/ana.410410512. Ann Neurol. 1997. PMID: 9153525

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