Small KW - Search Results

1

North Carolina macular dystrophy: exclusion map using RFLPs and microsatellites.

Small KW, Weber JL, Hung WY, Vance J, Roses A, Pericak-Vance M. Small KW, et al. Genomics. 1991 Nov;11(3):763-6. doi: 10.1016/0888-7543(91)90087-u. Genomics. 1991. PMID: 1685483

2

North Carolina macular dystrophy is assigned to chromosome 6.

Small KW, Weber JL, Roses A, Lennon F, Vance JM, Pericak-Vance MA. Small KW, et al. Genomics. 1992 Jul;13(3):681-5. doi: 10.1016/0888-7543(92)90141-e. Genomics. 1992. PMID: 1639395

3

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. Among authors: small kw. Genomics. 1990 Mar;6(3):565-7. doi: 10.1016/0888-7543(90)90488-g. Genomics. 1990. PMID: 2328994

4

North Carolina macular dystrophy (MCDR1). A review and refined mapping to 6q14-q16.2.

Small KW, Weber J, Roses A, Pericak-Vance P. Small KW, et al. Ophthalmic Paediatr Genet. 1993 Dec;14(4):143-50. doi: 10.3109/13816819309042913. Ophthalmic Paediatr Genet. 1993. PMID: 8015785 Review.

5

Genetic linkage studies of chromosome 17 RFLPs in von Recklinghausen neurofibromatosis (NF1).

Pericak-Vance MA, Yamaoka LH, Vance JM, Small K, Rosenwasser GO, Gaskell PC Jr, Hung WY, Alberts MJ, Haynes CS, Speer MC, et al. Pericak-Vance MA, et al. Genomics. 1987 Dec;1(4):349-52. doi: 10.1016/0888-7543(87)90036-x. Genomics. 1987. PMID: 3130305

6

Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias.

Damji KF, Allingham RR, Pollock SC, Small K, Lewis KE, Stajich JM, Yamaoka LH, Vance JM, Pericak-Vance MA. Damji KF, et al. Arch Neurol. 1996 Apr;53(4):338-44. doi: 10.1001/archneur.1996.00550040074016. Arch Neurol. 1996. PMID: 8929156 Review.

7

Genetic and physical map of 11 short tandem repeat polymorphisms on human chromosome 6.

Wilkie PJ, Polymeropoulos MH, Trent JM, Small KW, Weber JL. Wilkie PJ, et al. Among authors: small kw. Genomics. 1993 Jan;15(1):225-7. doi: 10.1006/geno.1993.1042. Genomics. 1993. PMID: 8432543 Free article.

8

Ocular motility in North Carolina autosomal dominant ataxia.

Small KW, Pollock SC, Vance JM, Stajich JM, Pericak-Vance M. Small KW, et al. J Neuroophthalmol. 1996 Jun;16(2):91-5. doi: 10.3109/01658109609009667. J Neuroophthalmol. 1996. PMID: 8797163

9

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. Among authors: small kw. 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.

10

North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysis.

Small KW, Udar N, Yelchits S, Klein R, Garcia C, Gallardo G, Puech B, Puech V, Saperstein D, Lim J, Haller J, Flaxel C, Kelsell R, Hunt D, Evans K, Lennon F, Pericak-Vance M. Small KW, et al. Mol Vis. 1999 Dec 29;5:38. Mol Vis. 1999. PMID: 10617775 Free article.

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