Martinsson T - Search Results

1

A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ovarian cancer family.

Nordling M, Karlsson P, Wahlström J, Engwall Y, Wallgren A, Martinsson T. Nordling M, et al. Among authors: martinsson t. Cancer Res. 1998 Apr 1;58(7):1372-5. Cancer Res. 1998. PMID: 9537232

2

An improved technique for chromosome preparations from human lymphocytes.

Johannesson T, Holmqvist D, Martinsson T, Wahlström J. Johannesson T, et al. Among authors: martinsson t. Hereditas. 1991;115(3):295-7. doi: 10.1111/j.1601-5223.1992.tb00573.x. Hereditas. 1991. PMID: 1816174 Free article. No abstract available.

3

Autism associated with marker chromosome.

Gillberg C, Steffenburg S, Wahlström J, Gillberg IC, Sjöstedt A, Martinsson T, Liedgren S, Eeg-Olofsson O. Gillberg C, et al. Among authors: martinsson t. J Am Acad Child Adolesc Psychiatry. 1991 May;30(3):489-94. doi: 10.1097/00004583-199105000-00022. J Am Acad Child Adolesc Psychiatry. 1991. PMID: 2055888

4

Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms.

Martinsson T, Sjöberg RM, Hedborg F, Kogner P. Martinsson T, et al. Cancer Res. 1995 Dec 1;55(23):5681-6. Cancer Res. 1995. PMID: 7585654

5

[von Hippel-Lindau hereditary tumor syndrome. Mutational analysis may improve prognosis].

Wiklund L, Nordling M, Engwall Y, Martinsson T, Szentgyörgyi E, Wahlström J. Wiklund L, et al. Among authors: martinsson t. Lakartidningen. 1995 Mar 15;92(11):1093-6. Lakartidningen. 1995. PMID: 7700111 Swedish.

6

Dilated cardiomyopathy and the dystrophin gene: an illustrated review.

Oldfors A, Eriksson BO, Kyllerman M, Martinsson T, Wahlström J. Oldfors A, et al. Among authors: martinsson t. Br Heart J. 1994 Oct;72(4):344-8. doi: 10.1136/hrt.72.4.344. Br Heart J. 1994. PMID: 7833192 Free PMC article. Review.

7

Linkage of a locus for carbohydrate-deficient glycoprotein syndrome type I (CDG1) to chromosome 16p, and linkage disequilibrium to microsatellite marker D16S406.

Martinsson T, Bjursell C, Stibler H, Kristiansson B, Skovby F, Jaeken J, Blennow G, Strömme P, Hanefeld F, Wahlström J. Martinsson T, et al. Hum Mol Genet. 1994 Nov;3(11):2037-42. Hum Mol Genet. 1994. PMID: 7874123

8

Progress in a genome scan for linkage in schizophrenia in a large Swedish kindred.

Barr CL, Kennedy JL, Pakstis AJ, Wetterberg L, Sjögren B, Bierut L, Wadelius C, Wahlström J, Martinsson T, Giuffra L, et al. Barr CL, et al. Among authors: martinsson t. Am J Med Genet. 1994 Mar 15;54(1):51-8. doi: 10.1002/ajmg.1320540110. Am J Med Genet. 1994. PMID: 7909991

9

HLA and prognosis in multiple sclerosis.

Runmarker B, Martinsson T, Wahlström J, Andersen O. Runmarker B, et al. Among authors: martinsson t. J Neurol. 1994 May;241(6):385-90. doi: 10.1007/BF02033356. J Neurol. 1994. PMID: 7931434

10

Duchenne muscular dystrophy and spinal muscular atrophy type I segregating in the same family.

Oldfors A, Martinsson T, Tessin I, Wahlström J, Wang S. Oldfors A, et al. Among authors: martinsson t. Clin Genet. 1994 Feb;45(2):97-103. doi: 10.1111/j.1399-0004.1994.tb04002.x. Clin Genet. 1994. PMID: 8004806

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