Authors:
FORSIUS H
DAMSTEN M
ERIKSSON AW
FELLMAN J
LINDH S
TAHVANAINEN E
Citation: H. Forsius et al., AUTOSOMAL RECESSIVE CORNEA PLANA - A CLINICAL AND GENETIC-STUDY OF 78CASES IN FINLAND, Acta ophthalmologica Scandinavica, 76(2), 1998, pp. 196-203
Authors:
TAHVANAINEN E
PAJUKANTA P
PORKKA K
NIEMINEN S
IKAVALKO L
NUOTIO I
TASKINEN MR
PELTONEN L
EHNHOLM C
Citation: E. Tahvanainen et al., HAPLOTYPES OF THE APOA-I C-III/A-IV GENE-CLUSTER AND FAMILIAL COMBINED HYPERLIPIDEMIA/, Arteriosclerosis, thrombosis, and vascular biology, 18(11), 1998, pp. 1810-1817
Authors:
TAHVANAINEN E
SYVANNE M
FRICK MH
MURTOMAKIREPO S
ANTIKAINEN M
KESANIEMI YA
KAUMA H
PASTERNAK A
TASKINEN MR
EHNHOLM C
Citation: E. Tahvanainen et al., ASSOCIATION OF VARIATION IN HEPATIC LIPASE ACTIVITY WITH PROMOTER VARIATION IN THE HEPATIC LIPASE GENE, The Journal of clinical investigation, 101(5), 1998, pp. 956-960
Authors:
TAHVANAINEN E
PAJUKANTA P
PORKKA K
NIEMINEN S
IKAVALKO L
NUOTIO I
TASKINEN MR
PELTONEN L
EHNHOLM C
Citation: E. Tahvanainen et al., HAPLOTYPES OF THE APOA-I C-III/A-IV GENE-CLUSTER AND FAMILIAL COMBINED HYPERLIPIDEMIA/, Atherosclerosis (Amsterdam), 138, 1998, pp. 55-55
Authors:
SIGLERVILLANUEVA A
TAHVANAINEN E
LINDH S
DIEGUEZLUCENA J
FORSIUS H
Citation: A. Siglervillanueva et al., AUTOSOMAL-DOMINANT CORNEA PLANA - CLINICAL FINDINGS IN A CUBAN FAMILYAND A REVIEW OF THE LITERATURE, Ophthalmic genetics, 18(2), 1997, pp. 55-62
Authors:
KOLEHMAINEN J
NORIO R
KIVITIEKALLIO S
TAHVANAINEN E
DELACHAPELLE A
LEHESJOKI AE
Citation: J. Kolehmainen et al., REFINED MAPPING OF THE COHEN-SYNDROME GENE BY LINKAGE DISEQUILIBRIUM, European journal of human genetics, 5(4), 1997, pp. 206-213
Authors:
TAHVANAINEN E
MURTOMAKIREPO S
ANTIKAINEN M
TIRET L
NICAUD V
JANSEN H
EHNHOLM C
Citation: E. Tahvanainen et al., A C-]T SUBSTITUTION AT THE POSITION -480 IN THE HEPATIC LIPASE GENE IS ASSOCIATED WITH HIGH SERUM HDL-CHOLESTEROL LEVEL IN FINNS, A RISK FACTOR FOR PREMATURE CORONARY HEART-DISEASE, Atherosclerosis, 134(1-2), 1997, pp. 27-27
Authors:
HUOPANIEMI L
RANTALA A
TAHVANAINEN E
DELACHAPELLE A
ALITALO T
Citation: L. Huopaniemi et al., LINKAGE DISEQUILIBRIUM AND PHYSICAL MAPPING OF X-LINKED JUVENILE RETINOSCHISIS, American journal of human genetics, 60(5), 1997, pp. 1139-1149
Authors:
TAHVANAINEN E
VILLANUEVA AS
FORSIUS H
SALO P
DELACHAPELLE A
Citation: E. Tahvanainen et al., DOMINANTLY AND RECESSIVELY INHERITED CORNEA PLANA CONGENITA MAP TO THE SAME SMALL REGION OF CHROMOSOME-12, PCR methods and applications, 6(4), 1996, pp. 249-254
Authors:
SAARI H
KOPONEN P
TAHVANAINEN E
LINDHOLM T
Citation: H. Saari et al., REMOTE READING AND DATA MANAGEMENT-SYSTEM FOR KWH METERS WITH POWER QUALITY MONITORING, Power engineering journal, 10(4), 1996, pp. 164-168
Authors:
WALLGRENPETTERSSON C
AVELA R
MARCHAND S
KOLEHMAINEN J
TAHVANAINEN E
HANSEN FJ
MUNTONI F
DUBOWITZ V
DEVISSER M
VANLANGEN IM
LAING NG
FAURE S
DELACHAPELLE A
Citation: C. Wallgrenpettersson et al., A GENE FOR AUTOSOMAL RECESSIVE NEMALINE MYOPATHY ASSIGNED TO CHROMOSOME 2Q BY LINKAGE ANALYSIS, Cytogenetics and cell genetics, 73(4), 1996, pp. 13-13
Authors:
ANTIKAINEN M
MURTOMAKI S
SYVANNE M
PAHLMAN R
TAHVANAINEN E
JAUHIAINEN M
FRICK MH
EHNHOLM C
Citation: M. Antikainen et al., THE GLN-ARG191 POLYMORPHISM OF THE HUMAN PARAOXONASE GENE (HUMPONA) IS NOT ASSOCIATED WITH THE RISK OF CORONARY-ARTERY DISEASE IN FINNS, The Journal of clinical investigation, 98(4), 1996, pp. 883-885
Authors:
WALLGRENPETTERSSON C
AVELA K
MARCHAND S
KOLEHMAINEN J
TAHVANAINEN E
HANSEN FJ
MUNTONI F
DUBOWITZ V
DEVISSER M
VANLANGEN IM
LAING NG
FAURE S
DELACHAPELLE A
Citation: C. Wallgrenpettersson et al., A GENE FOR AUTOSOMAL RECESSIVE NEMALINE MYOPATHY ASSIGNED TO CHROMOSOME 2Q BY LINKAGE ANALYSIS, Neuromuscular disorders, 5(6), 1995, pp. 441-443
Authors:
RANTA S
PIHKO H
SANTAVUORI P
TAHVANAINEN E
DELACHAPELLE A
Citation: S. Ranta et al., MUSCLE-EYE-BRAIN DISEASE AND FUKUYAMA TYPE CONGENITAL MUSCULAR-DYSTROPHY ARE NOT ALLELIC, Neuromuscular disorders, 5(3), 1995, pp. 221-225
Authors:
TAHVANAINEN E
FORSIUS H
KARILA E
RANTA S
EEROLA M
WEISSENBACH J
SISTONEN P
DELACHAPELLE A
Citation: E. Tahvanainen et al., CORNEA PLANA CONGENITA GENE ASSIGNED TO THE LONG ARM OF CHROMOSOME-12BY LINKAGE ANALYSIS, Genomics, 26(2), 1995, pp. 290-293
Authors:
RANTA S
TAHVANAINEN E
HIRVASNIEMI A
KARILA E
SISTONEN P
WEISSENBACH J
LEISTI J
LEHESJOKI AE
DELACHAPELLE A
Citation: S. Ranta et al., PROGRESSIVE EPILEPSY WITH MENTAL-RETARDATION MAPS TO THE TERMINAL REGION OF CHROMOSOME 8P, Cytogenetics and cell genetics, 68(3-4), 1995, pp. 160-161
Authors:
SALO P
IGNATIUS J
SIMOLA KOJ
TAHVANAINEN E
KAARIAINEN H
Citation: P. Salo et al., CLINICAL-FEATURES OF 9 MALES WITH MOLECULARLY DEFINED DELETIONS OF THE Y-CHROMOSOME LONG ARM, Journal of Medical Genetics, 32(9), 1995, pp. 711-715
Authors:
AMINOFF M
TAHVANAINEN E
GRASBECK R
WEISSENBACH J
BROCH H
DELACHAPELLE A
Citation: M. Aminoff et al., SELECTIVE INTESTINAL MALABSORPTION OF VITAMIN-B12 DISPLAYS RECESSIVE MENDELIAN INHERITANCE - ASSIGNMENT OF A LOCUS TO CHROMOSOME-10 BY LINKAGE, American journal of human genetics, 57(4), 1995, pp. 824-831
Authors:
TAHVANAINEN E
NORIO R
KARILA E
RANTA S
WEISSENBACH J
SISTONEN P
DELACHAPELLE A
Citation: E. Tahvanainen et al., COHEN SYNDROME GENE ASSIGNED TO THE LONG ARM OF CHROMOSOME-8 BY LINKAGE ANALYSIS, Nature genetics, 7(2), 1994, pp. 201-204
Authors:
TAHVANAINEN E
RANTA S
HIRVASNIEMI A
KARILA E
LEISTI J
SISTONEN P
WEISSENBACH J
LEHESJOKI AE
DELACHAPELLE A
Citation: E. Tahvanainen et al., THE GENE FOR A RECESSIVELY INHERITED HUMAN CHILDHOOD PROGRESSIVE EPILEPSY WITH MENTAL-RETARDATION MAPS TO THE DISTAL SHORT ARM OF CHROMOSOME-8, Proceedings of the National Academy of Sciences of the United Statesof America, 91(15), 1994, pp. 7267-7270
Authors:
TAHVANAINEN E
BEGGS AH
WALLGRENPETTERSSON C
Citation: E. Tahvanainen et al., EXCLUSION OF 2 CANDIDATE LOCI FOR AUTOSOMAL RECESSIVE NEMALINE MYOPATHY, Journal of Medical Genetics, 31(1), 1994, pp. 79-80