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Results: 1-25 |
Results: 25
AUTOSOMAL RECESSIVE CORNEA PLANA - A CLINICAL AND GENETIC-STUDY OF 78CASES IN FINLAND
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
HAPLOTYPES OF THE APOA-I C-III/A-IV GENE-CLUSTER AND FAMILIAL COMBINED HYPERLIPIDEMIA/
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
ASSOCIATION OF VARIATION IN HEPATIC LIPASE ACTIVITY WITH PROMOTER VARIATION IN THE HEPATIC LIPASE GENE
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
HAPLOTYPES OF THE APOA-I C-III/A-IV GENE-CLUSTER AND FAMILIAL COMBINED HYPERLIPIDEMIA/
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
AUTOSOMAL-DOMINANT CORNEA PLANA - CLINICAL FINDINGS IN A CUBAN FAMILYAND A REVIEW OF THE LITERATURE
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
HEPATIC LIPASE GENE POLYMORPHISMS INFLUENCE PLASMA HDL LEVELS - RESULTS FROM FINNISH EARS PARTICIPANTS
Authors: MURTOMAKI S TAHVANAINEN E ANTIKAINEN M TIRET L NICAUD V JANSEN H EHNHOLM C
Citation: S. Murtomaki et al., HEPATIC LIPASE GENE POLYMORPHISMS INFLUENCE PLASMA HDL LEVELS - RESULTS FROM FINNISH EARS PARTICIPANTS, Arteriosclerosis, thrombosis, and vascular biology, 17(10), 1997, pp. 1879-1884
REFINED MAPPING OF THE COHEN-SYNDROME GENE BY LINKAGE DISEQUILIBRIUM
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
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
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
HEPATIC LIPASE GENE POLYMORPHISMS IN CORONARY-ARTERY DISEASE PATIENTS
Authors: TAHVANAINEN E SYVANNE M MURTOMAKIREPO S TASKINEN MR KESANIEMI A PASTERNAK A EHNHOLM C
Citation: E. Tahvanainen et al., HEPATIC LIPASE GENE POLYMORPHISMS IN CORONARY-ARTERY DISEASE PATIENTS, Atherosclerosis, 134(1-2), 1997, pp. 27-27
LINKAGE DISEQUILIBRIUM AND PHYSICAL MAPPING OF X-LINKED JUVENILE RETINOSCHISIS
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
DOMINANTLY AND RECESSIVELY INHERITED CORNEA PLANA CONGENITA MAP TO THE SAME SMALL REGION OF CHROMOSOME-12
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
REMOTE READING AND DATA MANAGEMENT-SYSTEM FOR KWH METERS WITH POWER QUALITY MONITORING
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
A GENE FOR AUTOSOMAL RECESSIVE NEMALINE MYOPATHY ASSIGNED TO CHROMOSOME 2Q BY LINKAGE ANALYSIS
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
THE GENETICS OF CORNEA PLANA CONGENITA
Authors: TAHVANAINEN E FORSIUS H KOLEHMAINEN J DAMSTEN M FELLMAN J DELACHAPELLE A
Citation: E. Tahvanainen et al., THE GENETICS OF CORNEA PLANA CONGENITA, Journal of Medical Genetics, 33(2), 1996, pp. 116-119
THE GLN-ARG191 POLYMORPHISM OF THE HUMAN PARAOXONASE GENE (HUMPONA) IS NOT ASSOCIATED WITH THE RISK OF CORONARY-ARTERY DISEASE IN FINNS
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
A GENE FOR AUTOSOMAL RECESSIVE NEMALINE MYOPATHY ASSIGNED TO CHROMOSOME 2Q BY LINKAGE ANALYSIS
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
MUSCLE-EYE-BRAIN DISEASE AND FUKUYAMA TYPE CONGENITAL MUSCULAR-DYSTROPHY ARE NOT ALLELIC
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
LINKAGE DISEQUILIBRIUM MAPPING OF THE CORNEA PLANA CONGENITA GENE CNA2
Authors: TAHVANAINEN E FORSIUS H DAMSTEN M KARILA E KOLEHMAINEN J WEISSENBACH J SISTONEN P DELACHAPELLE A
Citation: E. Tahvanainen et al., LINKAGE DISEQUILIBRIUM MAPPING OF THE CORNEA PLANA CONGENITA GENE CNA2, Genomics, 30(3), 1995, pp. 409-414
CORNEA PLANA CONGENITA GENE ASSIGNED TO THE LONG ARM OF CHROMOSOME-12BY LINKAGE ANALYSIS
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
PROGRESSIVE EPILEPSY WITH MENTAL-RETARDATION MAPS TO THE TERMINAL REGION OF CHROMOSOME 8P
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
CLINICAL-FEATURES OF 9 MALES WITH MOLECULARLY DEFINED DELETIONS OF THE Y-CHROMOSOME LONG ARM
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
SELECTIVE INTESTINAL MALABSORPTION OF VITAMIN-B12 DISPLAYS RECESSIVE MENDELIAN INHERITANCE - ASSIGNMENT OF A LOCUS TO CHROMOSOME-10 BY LINKAGE
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
COHEN SYNDROME GENE ASSIGNED TO THE LONG ARM OF CHROMOSOME-8 BY LINKAGE ANALYSIS
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
THE GENE FOR A RECESSIVELY INHERITED HUMAN CHILDHOOD PROGRESSIVE EPILEPSY WITH MENTAL-RETARDATION MAPS TO THE DISTAL SHORT ARM OF CHROMOSOME-8
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
EXCLUSION OF 2 CANDIDATE LOCI FOR AUTOSOMAL RECESSIVE NEMALINE MYOPATHY
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
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