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European Journal of Human Genetics : EJHG|June 3, 1999
Y chromosomal polymorphisms reveal founding lineages in the Finns and the SaamiP Lahermo, M L Savontaus, P Sistonen, et al.
British Journal of Obstetrics and Gynaecology|May 1, 1983
Antenatal screening for congenital nephrosis in Finland by maternal serum alpha-fetoproteinM Ryynänen, M Seppälä, P Kuusela, et al.
Prenatal Diagnosis|August 19, 1999
Prenatal diagnosis of non-ketotic hyperglycinaemia: enzymatic diagnosis in 28 families and DNA diagnosis detecting prevalent Finnish and Israeli-Arab mutationsS Kure, M O Rolland, J Leisti, et al.
Human Genetics|September 1, 1995
Solid-phase minisequencing confirmed by FISH analysis in determination of gene copy numberM Laan, K Grön-Virta, A Salo, et al.
Neurology|January 1, 1983
Salla disease: a new lysosomal storage disorder with disturbed sialic acid metabolismM Renlund, P Aula, K O Raivio, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 1991
Spectrum of mutations in aspartylglucosaminuriaE Ikonen, P Aula, K Grön, et al.
Social Science & Medicine (1982)|July 17, 1998
Attitudes towards genetic testing: analysis of contradictionsP Jallinoja, A Hakonen, A R Aro, et al.
American Journal of Human Genetics|August 19, 2000
The spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlationN Aula, P Salomäki, R Timonen, et al.
Archives of Neurology|February 1, 1979
"Salla disease": a new lysosomal storage disorderP Aula, S Autio, K O Raivio, et al.
The EMBO Journal|January 1, 1991
Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the diseaseE Ikonen, M Baumann, K Grön, et al.
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