Sistonen P - Search Results

1

Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysis.

Avela K, Lipsanen-Nyman M, Perheentupa J, Wallgren-Pettersson C, Marchand S, Fauré S, Sistonen P, de la Chapelle A, Lehesjoki AE. Avela K, et al. Among authors: sistonen p. Am J Hum Genet. 1997 Apr;60(4):896-902. Am J Hum Genet. 1997. PMID: 9106536 Free PMC article.

2

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland.

Hästbacka J, de la Chapelle A, Kaitila I, Sistonen P, Weaver A, Lander E. Hästbacka J, et al. Among authors: sistonen p. Nat Genet. 1992 Nov;2(3):204-11. doi: 10.1038/ng1192-204. Nat Genet. 1992. PMID: 1345170

3

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

4

Hemophilia A: genetic prediction and linkage studies in all available families in Finland.

Lehesjoki AE, Sistonen P, Rasi V, de la Chapelle A. Lehesjoki AE, et al. Among authors: sistonen p. Clin Genet. 1991 Mar;39(3):199-209. doi: 10.1111/j.1399-0004.1991.tb03012.x. Clin Genet. 1991. PMID: 2036741

5

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

6

Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium.

Höglund P, Sistonen P, Norio R, Holmberg C, Dimberg A, Gustavson KH, de la Chapelle A, Kere J. Höglund P, et al. Among authors: sistonen p. Am J Hum Genet. 1995 Jul;57(1):95-102. Am J Hum Genet. 1995. PMID: 7611301 Free PMC article.

7

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

8

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

9

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.

10

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

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