Thompson AD - Search Results

1

YAC and cosmid contigs spanning the Batten disease (CLN3) region at 16p12.1-p11.2.

Järvelä IE, Mitchison HM, O'Rawe AM, Munroe PB, Taschner PE, de Vos N, Lerner TJ, D'Arigo KL, Callen DF, Thompson AD, et al. Järvelä IE, et al. Among authors: thompson ad. Genomics. 1995 Sep 20;29(2):478-89. doi: 10.1006/geno.1995.9978. Genomics. 1995. PMID: 8666398

2

Fine genetic mapping of the Batten disease locus (CLN3) by haplotype analysis and demonstration of allelic association with chromosome 16p microsatellite loci.

Mitchison HM, Thompson AD, Mulley JC, Kozman HM, Richards RI, Callen DF, Stallings RL, Doggett NA, Attwood J, McKay TR, et al. Mitchison HM, et al. Among authors: thompson ad. Genomics. 1993 May;16(2):455-60. doi: 10.1006/geno.1993.1210. Genomics. 1993. PMID: 8314582

3

Refined localization of the Batten disease gene (CLN3) by haplotype and linkage disequilibrium mapping to D16S288-D16S383 and exclusion from this region of a variant form of Batten disease with granular osmiophilic deposits.

Mitchison HM, O'Rawe AM, Lerner TJ, Taschner PE, Schlumpf K, D'Arigo K, de Vos N, Gormally E, Phillips HA, Thompson AD, et al. Mitchison HM, et al. Among authors: thompson ad. Am J Med Genet. 1995 Jun 5;57(2):312-5. doi: 10.1002/ajmg.1320570241. Am J Med Genet. 1995. PMID: 7668353

4

Genetic mapping of the Batten disease locus (CLN3) to the interval D16S288-D16S383 by analysis of haplotypes and allelic association.

Mitchison HM, Taschner PE, O'Rawe AM, de Vos N, Phillips HA, Thompson AD, Kozman HM, Haines JL, Schlumpf K, D'Arigo K, et al. Mitchison HM, et al. Among authors: thompson ad. Genomics. 1994 Jul 15;22(2):465-8. doi: 10.1006/geno.1994.1412. Genomics. 1994. PMID: 7806237

5

Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12.

Callen DF, Baker E, Lane S, Nancarrow J, Thompson A, Whitmore SA, MacLennan DH, Berger R, Cherif D, Järvelä I, et al. Callen DF, et al. Am J Hum Genet. 1991 Dec;49(6):1372-7. Am J Hum Genet. 1991. PMID: 1746562 Free PMC article.

6

Genetic heterogeneity in neuronal ceroid lipofuscinosis (NCL): evidence that the late-infantile subtype (Jansky-Bielschowsky disease; CLN2) is not an allelic form of the juvenile or infantile subtypes.

Williams R, Vesa J, Järvelä I, McKay T, Mitchison H, Hellsten E, Thompson A, Callen D, Sutherland G, Luna-Battadano D, et al. Williams R, et al. Am J Hum Genet. 1993 Oct;53(4):931-5. Am J Hum Genet. 1993. PMID: 8213822 Free PMC article.

7

High-resolution cytogenetic-based physical map of human chromosome 16.

Callen DF, Doggett NA, Stallings RL, Chen LZ, Whitmore SA, Lane SA, Nancarrow JK, Apostolou S, Thompson AD, Lapsys NM, et al. Callen DF, et al. Among authors: thompson ad. Genomics. 1992 Aug;13(4):1178-85. doi: 10.1016/0888-7543(92)90035-q. Genomics. 1992. PMID: 1505951

8

Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16.

Thompson AD, Shen Y, Holman K, Sutherland GR, Callen DF, Richards RI. Thompson AD, et al. Genomics. 1992 Jun;13(2):402-8. doi: 10.1016/0888-7543(92)90260-y. Genomics. 1992. PMID: 1612599

9

Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease).

Taschner PE, de Vos N, Thompson AD, Callen DF, Doggett N, Mole SE, Dooley TP, Barth PG, Breuning MH. Taschner PE, et al. Among authors: thompson ad. Am J Hum Genet. 1995 Mar;56(3):663-8. Am J Hum Genet. 1995. PMID: 7887420 Free PMC article.

10

Refined genetic mapping of juvenile-onset neuronal ceroid-lipofuscinosis on chromosome 16.

Mitchison HM, Williams RE, McKay TR, Callen DF, Thompson AD, Mulley JC, Stallings RL, Hildebrand CE, Moyzis RK, Järvelä I, et al. Mitchison HM, et al. Among authors: thompson ad. J Inherit Metab Dis. 1993;16(2):339-41. doi: 10.1007/BF00710278. J Inherit Metab Dis. 1993. PMID: 8105142 No abstract available.

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