On the heritability of serum high density lipoprotein in twins.

per Sistonen, P, Ehnholm, C
Publicat 1980

Haplotype analysis in prenatal diagnosis and carrier identification of Salla disease.

per Schleutker, J, Sistonen, P, Aula, P
Publicat 1996

Diastrophic dysplasia gene maps to the distal long arm of chromosome 5.

per Hästbacka, J, Kaitila, I, Sistonen, P, de la Chapelle, A
Publicat 1990

The gene for congenital chloride diarrhea maps close to but is distinct from the gene for cystic fibrosis transmembrane conductance regulator.

per Kere, J, Sistonen, P, Holmberg, C, de la Chapelle, A
Publicat 1993

Screening for microsatellite instability target genes in colorectal cancers

per Vilkki, S, Launonen, V, Karhu, A, Sistonen, P, Vastrik, I, Aaltonen, L
Publicat 2002

Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer.

per Moisio, A. L., Sistonen, P., Weissenbach, J., de la Chapelle, A., Peltomäki, P.
Publicat 1996

Genome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22

per Pulli, K, Karma, K, Norio, R, Sistonen, P, Göring, H H H, Järvelä, I
Publicat 2008

The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNA.

per Lahermo, P., Sajantila, A., Sistonen, P., Lukka, M., Aula, P., Peltonen, L., Savontaus, M. L.
Publicat 1996

Lysinuric protein intolerance (LPI) gene maps to the long arm of chromosome 14.

per Lauteala, T, Sistonen, P, Savontaus, M L, Mykkänen, J, Simell, J, Lukkarinen, M, Simell, O, Aula, P
Publicat 1997

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

per Sulisalo, T., Klockars, J., Mäkitie, O., Francomano, C. A., de la Chapelle, A., Kaitila, I., Sistonen, P.
Publicat 1994

Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22.

per Lehesjoki, A E, Koskiniemi, M, Sistonen, P, Miao, J, Hästbacka, J, Norio, R, de la Chapelle, A
Publicat 1991

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

per Höglund, P, Sistonen, P, Norio, R, Holmberg, C, Dimberg, A, Gustavson, K H, de la Chapelle, A, Kere, J
Publicat 1995

Subpopulation difference scanning: a strategy for exclusion mapping of susceptibility genes

per Salmela, E, Taskinen, O, Seppänen, J K, Sistonen, P, Daly, M J, Lahermo, P, Savontaus, M‐L, Kere, J
Publicat 2006

The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8.

per Tahvanainen, E, Ranta, S, Hirvasniemi, A, Karila, E, Leisti, J, Sistonen, P, Weissenbach, J, Lehesjoki, A E, de la Chapelle, A
Publicat 1994

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

per Avela, K, Lipsanen-Nyman, M, Perheentupa, J, Wallgren-Pettersson, C, Marchand, S, Fauré, S, Sistonen, P, de la Chapelle, A, Lehesjoki, A E
Publicat 1997

Frequent loss of SMAD4/DPC4 protein in colorectal cancers

per Salovaara, R, Roth, S, Loukola, A, Launonen, V, Sistonen, P, Avizienyte, E, Kristo, P, Järvinen, H, Souchelnytskyi, S, Sarlomo-Rikala, M, Aaltonen, L A
Publicat 2002

Frequent loss of SMAD4/DPC4 protein in colorectal cancers

per Salovaara, R, Roth, S, Loukola, A, Launonen, V, Sistonen, P, Avizienyte, E, Kristo, P, Järvinen, H, Souchelnytskyi, S, Sarlomo-Rikala, M, Aaltonen, L A
Publicat 2002

Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer families.

per Nyström-Lahti, M, Sistonen, P, Mecklin, J P, Pylkkänen, L, Aaltonen, L A, Järvinen, H, Weissenbach, J, de la Chapelle, A, Peltomäki, P
Publicat 1994