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Kidney International|April 1, 1985
Accumulation of laminin and type IV collagen in the kidney in congenital nephrosisH Autio-Harmainen, T Karttunen, L Risteli, et al.
Birth Defects Original Article Series|January 1, 1975
Mulibrey nanism: review of 23 cases of a new autosomal recessive syndromeJ Perheentupa, S Autio, S Leisti, et al.
British Medical Journal (Clinical Research Ed.)|August 11, 1984
Risk of minor and major fetal malformations in diabetics with high haemoglobin A1c values in early pregnancyK Ylinen, P Aula, U H Stenman, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|October 1, 1992
Autophagy, cathepsin L transport, and acidification in cultured rat fibroblastsE L Punnonen, S Autio, V S Marjomäki, et al.
Clinical Genetics|August 1, 1985
Partial trisomy 12q: clinical and cytogenetic observationsC Tengström, M Wilska, M Kähkönen, et al.
Human Genetics|January 1, 1992
Exclusion map of Salla disease: attempts to localize the disease gene using a computer programL Haataja, J Schleutker, M Renlund, et al.
American Journal of Medical Genetics|March 17, 1997
New progeroid disorderM Penttinen, K M Niemi, H Vinkka-Puhakka, et al.
The Journal of Clinical Investigation|April 1, 1991
Sialic acid storage diseases. A multiple lysosomal transport defect for acidic monosaccharidesG M Mancini, C E Beerens, P P Aula, et al.
Genomics|November 1, 1990
Analysis of mitochondrial ND4 gene DNA sequence in Finnish families with Leber hereditary optic neuroretinopathyK Huoponen, J Vilkki, M L Savontaus, et al.
Acta Neurologica Scandinavica|May 1, 1993
Epileptic seizures in aspartylglucosaminuria: a common disorderM Arvio, V Oksanen, S Autio, et al.
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