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Human Genetics|July 1, 1990
Linkage of aspartylglucosaminuria (AGU) to marker loci on the long arm of chromosome 4K Grön, P Aula, L PeltonenHuman Genetics|February 1, 1994
Diagnosis of fragile X syndrome by direct mutation analysisM L Väisänen, M Kähkönen, J LeistiNeuropediatrics|November 1, 1980
Cry analysis of infants with karyotype abnormalityK Michelsson, N Tuppurainen, P AulaAmerican Journal of Human Genetics|September 1, 1996
Decrease in the CGGn trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmissionM L Väisänen, R Haataja, J LeistiJournal of Medical Genetics|May 23, 1998
Myotonia congenita in northern Finland: an epidemiological and genetic studyP Baumann, V V Myllylä, J LeistiAmerican Journal of Medical Genetics|April 1, 1992
Carrier detection of the fragile X syndrome with flanking RFLP markers and linkage analysisM L Väisänen, M Kähkönen, J LeistiJournal of Inherited Metabolic Disease|January 1, 1980
Variation of urinary excretion of aspartylglucosamine and associated clinical findings in aspartyglucosaminuriaP Aula, K O Raivio, P MauryVirchows Archiv. B, Cell Pathology|September 11, 1975
Distribution of cytoplasmic vacuoles in blood T and B lymphocytes in two lysosomal disordersP Aula, J Rapola, L C AnderssonClinical Genetics|July 1, 1980
Fetal gonadal histology in XXXXY, XYY and XXX syndromesH Autio-Harmainen, J Rapola, P AulaAmerican Journal of Medical Genetics|March 1, 1985
A lethal autosomal recessive syndrome of multiple congenital contracturesR Herva, J Leisti, P Kirkinen, et al.Pageof 17