NS01289/NS/NINDS NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1989	1
1990	1
1991	3
1992	1
1993	4
1994	1
2024	0

1

Hereditary motor and sensory neuropathies.

Vance JM. Vance JM. J Med Genet. 1991 Jan;28(1):1-5. doi: 10.1136/jmg.28.1.1. J Med Genet. 1991. PMID: 1999826 Free PMC article. Review. No abstract available.

2

Confirmation of linkage in von Hippel-Lindau disease.

Vance JM, Small KW, Jones MA, Stajich JM, Yamaoka LH, Roses AD, Hung WY, Pericak-Vance MA. Vance JM, et al. Genomics. 1990 Mar;6(3):565-7. doi: 10.1016/0888-7543(90)90488-g. Genomics. 1990. PMID: 2328994

3

Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.

Vance JM, Barker D, Yamaoka LH, Stajich JM, Loprest L, Hung WY, Fischbeck K, Roses AD, Pericak-Vance MA. Vance JM, et al. Genomics. 1991 Apr;9(4):623-8. doi: 10.1016/0888-7543(91)90355-i. Genomics. 1991. PMID: 1674726

4

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.

Ben Othmane K, Hentati F, Lennon F, Ben Hamida C, Blel S, Roses AD, Pericak-Vance MA, Ben Hamida M, Vance JM. Ben Othmane K, et al. Hum Mol Genet. 1993 Oct;2(10):1625-8. doi: 10.1093/hmg/2.10.1625. Hum Mol Genet. 1993. PMID: 8268915

5

Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17.

Vance JM, Nicholson GA, Yamaoka LH, Stajich J, Stewart CS, Speer MC, Hung WY, Roses AD, Barker D, Pericak-Vance MA. Vance JM, et al. Exp Neurol. 1989 May;104(2):186-9. doi: 10.1016/s0014-4886(89)80013-5. Exp Neurol. 1989. PMID: 2707366

6

Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entities.

Loprest LJ, Pericak-Vance MA, Stajich J, Gaskell PC, Lucas AM, Lennon F, Yamaoka LH, Roses AD, Vance JM. Loprest LJ, et al. Neurology. 1992 Mar;42(3 Pt 1):597-601. doi: 10.1212/wnl.42.3.597. Neurology. 1992. PMID: 1549221

7

Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26.

Pericak-Vance MA, Nunes KJ, Whisenant E, Loeb DB, Small KW, Stajich JM, Rimmler JB, Yamaoka LH, Smith DI, Drabkin HA, et al. Pericak-Vance MA, et al. J Med Genet. 1993 Jun;30(6):487-91. doi: 10.1136/jmg.30.6.487. J Med Genet. 1993. PMID: 8100855 Free PMC article.

8

Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity.

Ben Othmane K, Middleton LT, Loprest LJ, Wilkinson KM, Lennon F, Rozear MP, Stajich JM, Gaskell PC, Roses AD, Pericak-Vance MA, et al. Ben Othmane K, et al. Genomics. 1993 Aug;17(2):370-5. doi: 10.1006/geno.1993.1334. Genomics. 1993. PMID: 8406488

9

A PvuII polymorphism detected by pEW404 (D17S64) on chromosome 17.

Lucas AM, Vance JM, Stajich JM, Roses AD. Lucas AM, et al. Nucleic Acids Res. 1991 Oct 25;19(20):5802. doi: 10.1093/nar/19.20.5802-a. Nucleic Acids Res. 1991. PMID: 1682890 Free PMC article. No abstract available.

10

Dinucleotide repeat polymorphisms in the VHL region of human chromosome 3p25.

Loeb D, Lui W, Smith DI, Vance JM. Loeb D, et al. Hum Mol Genet. 1993 Oct;2(10):1746. doi: 10.1093/hmg/2.10.1746. Hum Mol Genet. 1993. PMID: 8268940 No abstract available.

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