Raskind WH - Search Results

1

Frequent loss of heterozygosity for markers on chromosome arm 10q in chondrosarcomas.

Raskind WH, Conrad EU, Matsushita M. Raskind WH, et al. Genes Chromosomes Cancer. 1996 Jun;16(2):138-43. doi: 10.1002/(SICI)1098-2264(199606)16:2<138::AID-GCC8>3.0.CO;2-0. Genes Chromosomes Cancer. 1996. PMID: 8818661

2

Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11.

Raskind WH, Conrad EU, Chansky H, Matsushita M. Raskind WH, et al. Am J Hum Genet. 1995 May;56(5):1132-9. Am J Hum Genet. 1995. PMID: 7726169 Free PMC article.

3

A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.

Brkanac Z, Bylenok L, Fernandez M, Matsushita M, Lipe H, Wolff J, Nochlin D, Raskind WH, Bird TD. Brkanac Z, et al. Among authors: raskind wh. Arch Neurol. 2002 Aug;59(8):1291-5. doi: 10.1001/archneur.59.8.1291. Arch Neurol. 2002. PMID: 12164726

4

Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.

Chapman NH, Igo RP, Thomson JB, Matsushita M, Brkanac Z, Holzman T, Berninger VW, Wijsman EM, Raskind WH. Chapman NH, et al. Among authors: raskind wh. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):67-75. doi: 10.1002/ajmg.b.30018. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15389770

5

Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21.

Raskind WH, Matsushita M, Peter B, Biberston J, Wolff J, Lipe H, Burbank R, Bird TD. Raskind WH, et al. Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 5;150B(4):570-4. doi: 10.1002/ajmg.b.30879. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18980218 Free PMC article.

6

Hereditary benign chorea: clinical and genetic features of a distinct disease.

Fernandez M, Raskind W, Matsushita M, Wolff J, Lipe H, Bird T. Fernandez M, et al. Neurology. 2001 Jul 10;57(1):106-10. doi: 10.1212/wnl.57.1.106. Neurology. 2001. PMID: 11445636

7

The natural history of hereditary multiple exostoses.

Schmale GA, Conrad EU 3rd, Raskind WH. Schmale GA, et al. Among authors: raskind wh. J Bone Joint Surg Am. 1994 Jul;76(7):986-92. doi: 10.2106/00004623-199407000-00005. J Bone Joint Surg Am. 1994. PMID: 8027127

8

Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34.

Raskind WH, Bolin T, Wolff J, Fink J, Matsushita M, Litt M, Lipe H, Bird TD. Raskind WH, et al. Hum Genet. 1998 Jan;102(1):93-7. doi: 10.1007/s004390050659. Hum Genet. 1998. PMID: 9490305 Free article.

9

Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses.

Raskind WH, Conrad EU 3rd, Matsushita M, Wijsman EM, Wells DE, Chapman N, Sandell LJ, Wagner M, Houck J. Raskind WH, et al. Hum Mutat. 1998;11(3):231-9. doi: 10.1002/(SICI)1098-1004(1998)11:3<231::AID-HUMU8>3.0.CO;2-K. Hum Mutat. 1998. PMID: 9521425

10

Expression of cartilage extracellular matrix and potential regulatory genes in a new human chondrosarcoma cell line.

Chansky H, Robbins JR, Cha S, Raskind WH, Conrad EU, Sandell LJ. Chansky H, et al. Among authors: raskind wh. J Orthop Res. 1998 Sep;16(5):521-30. doi: 10.1002/jor.1100160502. J Orthop Res. 1998. PMID: 9820274

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