Sistonen P - Search Results

1

Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.

Sankila EM, Pakarinen L, Kääriäinen H, Aittomäki K, Karjalainen S, Sistonen P, de la Chapelle A. Sankila EM, et al. Among authors: sistonen p. Hum Mol Genet. 1995 Jan;4(1):93-8. doi: 10.1093/hmg/4.1.93. Hum Mol Genet. 1995. PMID: 7711740

2

Choroideremia: linkage analysis with physically mapped close DNA-markers.

Sankila EM, Sistonen P, Cremers F, de la Chapelle A. Sankila EM, et al. Among authors: sistonen p. Hum Genet. 1991 Jul;87(3):348-52. doi: 10.1007/BF00200918. Hum Genet. 1991. PMID: 1677924

3

Linked polymorphic DNA markers in the prediction of X-linked muscular dystrophy.

Lindlöf M, Sistonen P, de la Chapelle A. Lindlöf M, et al. Among authors: sistonen p. Ann Hum Genet. 1987 Oct;51(4):317-28. doi: 10.1111/j.1469-1809.1987.tb01066.x. Ann Hum Genet. 1987. PMID: 3482147

4

Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis.

Tahvanainen E, Norio R, Karila E, Ranta S, Weissenbach J, Sistonen P, de la Chapelle A. Tahvanainen E, et al. Among authors: sistonen p. Nat Genet. 1994 Jun;7(2):201-4. doi: 10.1038/ng0694-201. Nat Genet. 1994. PMID: 7920642

5

High-resolution linkage-disequilibrium mapping of the cartilage-hair hypoplasia gene.

Sulisalo T, Klockars J, Mäkitie O, Francomano CA, de la Chapelle A, Kaitila I, Sistonen P. Sulisalo T, et al. Among authors: sistonen p. Am J Hum Genet. 1994 Nov;55(5):937-45. Am J Hum Genet. 1994. PMID: 7977356 Free PMC article.

6

Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis.

Sulisalo T, Sistonen P, Hästbacka J, Wadelius C, Mäkitie O, de la Chapelle A, Kaitila I. Sulisalo T, et al. Among authors: sistonen p. Nat Genet. 1993 Apr;3(4):338-41. doi: 10.1038/ng0493-338. Nat Genet. 1993. PMID: 7981754

7

Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping.

Lehesjoki AE, Koskiniemi M, Norio R, Tirrito S, Sistonen P, Lander E, de la Chapelle A. Lehesjoki AE, et al. Among authors: sistonen p. Hum Mol Genet. 1993 Aug;2(8):1229-34. doi: 10.1093/hmg/2.8.1229. Hum Mol Genet. 1993. PMID: 8104628

8

Genetic mapping of the erythropoietin receptor gene.

Sistonen P, Träskelin AL, Lehväslaiho H, de la Chapelle A. Sistonen P, et al. Hum Genet. 1993 Oct 1;92(3):299-301. doi: 10.1007/BF00244476. Hum Genet. 1993. PMID: 8406437

9

Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q.

Virtaneva K, Miao J, Träskelin AL, Stone N, Warrington JA, Weissenbach J, Myers RM, Cox DR, Sistonen P, de la Chapelle A, et al. Virtaneva K, et al. Among authors: sistonen p. Am J Hum Genet. 1996 Jun;58(6):1247-53. Am J Hum Genet. 1996. PMID: 8651302 Free PMC article.

10

Refined mapping of the Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous region.

Joensuu T, Blanco G, Pakarinen L, Sistonen P, Kääriäinen H, Brown S, Chapelle A, Sankila EM. Joensuu T, et al. Among authors: sistonen p. Genomics. 1996 Dec 15;38(3):255-63. doi: 10.1006/geno.1996.0626. Genomics. 1996. PMID: 8975700

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