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Results: 26-31/31
Authors:
JUVONEN V
HUOPONEN K
SYVANEN AC
NIKOSKELAINEN E
SAVONTAUS ML
Citation: V. Juvonen et al., QUANTIFICATION OF POINT MUTATIONS ASSOCIATED WITH LEBER HEREDITARY OPTIC NEURORETINOPATHY BY SOLID-PHASE MINISEQUENCING, Human genetics, 93(1), 1994, pp. 16-20
Authors:
SYVANEN AC
Citation: Ac. Syvanen, DETECTION OF POINT MUTATIONS IN HUMAN GENES BY THE SOLID-PHASE MINISEQUENCING METHOD, Clinica chimica acta, 226(2), 1994, pp. 225-236
Authors:
SUOMALAINEN A
MAJANDER A
PIHKO H
PELTONEN L
SYVANEN AC
Citation: A. Suomalainen et al., QUANTIFICATION OF TRANSFER RNA(3243)(LEU) POINT MUTATION OF MITOCHONDRIAL-DNA IN MELAS PATIENTS AND ITS EFFECTS ON MITOCHONDRIAL TRANSCRIPTION, Human molecular genetics, 2(5), 1993, pp. 525-534
Authors:
HALILA R
IKONEN E
TOLLERSRUD O
SYVANEN AC
ENOMAA N
PELTONEN L
Citation: R. Halila et al., ASPARTYLGLUCOSAMINURIA (AGU) - PROTEIN AND GENE STRUCTURE OF NORMAL AND MUTATED ASPARTYLGLUCOSAMINIDASE, Biochemical medicine and metabolic biology, 50(1), 1993, pp. 1-8
Authors:
IKONEN E
SYVANEN AC
PELTONEN L
Citation: E. Ikonen et al., DISSECTION OF THE MOLECULAR PATHOLOGY OF ASPARTYLGLUCOSAMINURIA PROVIDES THE BASIS FOR DNA DIAGNOSTICS AND FUTURE THERAPEUTIC INTERVENTIONS, Scandinavian journal of clinical & laboratory investigation, 53, 1993, pp. 19-27
Authors:
PALOTIE A
SYVANEN AC
Citation: A. Palotie et Ac. Syvanen, DEVELOPMENT OF MOLECULAR-GENETIC METHODS FOR MONITORING MYELOID MALIGNANCIES, Scandinavian journal of clinical & laboratory investigation, 53, 1993, pp. 29-38