Small K - Search Results

1

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. Among authors: small k. Arch Neurol. 1996 Apr;53(4):338-44. doi: 10.1001/archneur.1996.00550040074016. Arch Neurol. 1996. PMID: 8929156 Review.

2

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

3

Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type I.

Vance JM, Pericak-Vance MA, Yamaoka LH, Speer MC, Rosenwasser GO, Small K, Gaskell PC Jr, Hung WY, Alberts MJ, Haynes CS, et al. Vance JM, et al. Among authors: small k. Am J Hum Genet. 1989 Jan;44(1):25-9. Am J Hum Genet. 1989. PMID: 2491777 Free PMC article.

4

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. Among authors: small k. Genomics. 1987 Dec;1(4):349-52. doi: 10.1016/0888-7543(87)90036-x. Genomics. 1987. PMID: 3130305

5

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

6

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

7

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

8

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.

9

Optic atrophy in primary oxalosis.

Small KW, Pollock S, Scheinman J. Small KW, et al. Am J Ophthalmol. 1988 Jul 15;106(1):96-7. doi: 10.1016/s0002-9394(14)76398-6. Am J Ophthalmol. 1988. PMID: 3394775 No abstract available.

10

Blepharophimosis syndrome is linked to chromosome 3q.

Small KW, Stalvey M, Fisher L, Mullen L, Dickel C, Beadles K, Reimer R, Lessner A, Lewis K, Pericak-Vance MA. Small KW, et al. Hum Mol Genet. 1995 Mar;4(3):443-8. doi: 10.1093/hmg/4.3.443. Hum Mol Genet. 1995. PMID: 7795600

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

493 results

Search Page