Showing results (11-20 of 21) with videos related to
Sort By:
Pageof 3
Clinical Genetics|September 5, 2001
Risk of obstetric cholestasis in sisters of index patientsM L Eloranta, S Heinonen, T Mononen, et al.Analytical Biochemistry|February 1, 1993
A fluorometric assay for glycosylasparaginase activity and detection of aspartylglycosaminuriaI T Mononen, V M Kaartinen, J C WilliamsClinical Genetics|October 10, 2007
A novel duplication in the FMR1 gene: implications for molecular analysis in fragile X syndrome and repeat instabilityT Mononen, H von Koskull, R-L Airaksinen, et al.Acta Paediatrica (Oslo, Norway : 1992)|March 1, 1995
A population-based study on the causes of mild and severe mental retardationR Matilainen, E Airaksinen, T Mononen, et al.Clinical Chemistry|March 1, 1994
Enzymatic diagnosis of aspartylglycosaminuria by fluorometric assay of glycosylasparaginase in serum, plasma, or lymphocytesI Mononen, T Mononen, P Ylikangas, et al.The American Journal of Clinical Nutrition|June 1, 1986
Plasma vitamin C levels are low in premature infants fed human milkK Heinonen, I Mononen, T Mononen, et al.Archives of Orthopaedic and Trauma Surgery|January 1, 1997
Instrumented measurement of anterior-posterior translation in knees with chronic anterior cruciate ligament tearT Mononen, H Alaranta, A Harilainen, et al.The Journal of Biological Chemistry|February 15, 1992
Aspartylglycosaminuria in a non-Finnish patient caused by a donor splice mutation in the glycoasparaginase geneI Mononen, N Heisterkamp, V Kaartinen, et al.Clinical Chemistry|January 1, 1995
Finnish-type aspartylglucosaminuria detected by oligonucleotide ligation assayC M Delahunty, W Ankener, S Brainerd, et al.Epilepsia|September 22, 2000
A population-based study on epilepsy in mentally retarded childrenE M Airaksinen, R Matilainen, T Mononen, et al.Pageof 3