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Citation: Ra. Philibert et al., THE CHARACTERIZATION AND SEQUENCE-ANALYSIS OF 30 CTG-REPEAT CONTAINING GENOMIC COSMID CLONES, European journal of human genetics, 6(1), 1998, pp. 89-94
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Citation: K. Avela et al., CONSTRUCTION OF A PHYSICAL MAP IN THE MECKEL-SYNDROME AND MULIBREY NANISM CRITICAL REGION ON CHROMOSOME 17Q22, European journal of human genetics, 6, 1998, pp. 4100-4100
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Citation: U. Wartiovaara et al., PERIPHERAL-BLOOD PLATELETS EXPRESS VEGF-C AND VEGF WHICH ARE RELEASEDDURING PLATELET ACTIVATION, Thrombosis and haemostasis, 80(1), 1998, pp. 171-175
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Citation: U. Wartiovaara et al., ASSOCIATION OF FXIIIV34L WITH LOWER INCIDENCE OF MYOCARDIAL-INFARCTION IN FINNISH MALES WITH CORONARY-ARTERY DISEASE, British Journal of Haematology, 102(1), 1998, pp. 147-147
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Citation: I. Visapaa et al., ASSIGNMENT OF THE LOCUS FOR A NEW LETHAL NEONATAL METABOLIC SYNDROME TO 2Q33-37, American journal of human genetics, 63(5), 1998, pp. 1396-1403
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Citation: P. Makelabengs et al., ASSIGNMENT OF THE DISEASE LOCUS FOR LETHAL CONGENITAL CONTRACTURE SYNDROME TO A RESTRICTED REGION OF CHROMOSOME 9Q34, BY GENOME SCAN USING 5 AFFECTED INDIVIDUALS, American journal of human genetics, 63(2), 1998, pp. 506-516
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Citation: J. Aaltonen et al., AN AUTOIMMUNE-DISEASE, APECED, CAUSED BY MUTATIONS IN A NOVEL GENE FEATURING 2 PHD-TYPE ZINC-FINGER DOMAINS, Nature genetics, 17(4), 1997, pp. 399-403
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Citation: P. Suvanto et al., CLONING, MESSENGER-RNA DISTRIBUTION AND CHROMOSOMAL LOCALIZATION OF THE GENE FOR GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR-RECEPTOR-BETA,A HOMOLOG TO GDNFR-ALPHA, Human molecular genetics, 6(8), 1997, pp. 1267-1273
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Citation: N. Horellikuitunen et al., THE ORDER AND TRANSCRIPTIONAL ORIENTATION OF THE HUMAN COL13A1 AND P4HA GENES ON CHROMOSOME-10 LONG ARM DETERMINED BY HIGH-RESOLUTION FISH, Genomics, 46(2), 1997, pp. 299-302
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Citation: Hm. Helander et al., MOLECULAR-CLONING AND CHARACTERIZATION OF THE HUMAN MITOCHONDRIAL 2,4-DIENOYL-COA REDUCTASE GENE (DECR), Genomics, 46(1), 1997, pp. 112-119
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Citation: T. Klockars et al., THE VISUAL ASSIGNMENT OF GENES BY FIBER-FISH - BTF3 PROTEIN HOMOLOG GENE (BTF3) AND A NOVEL PSEUDOGENE OF HUMAN RNA HELICASE-A (DDX9P) ON 13Q22 (VOL 44, PG 355, 1997), Genomics, 46(1), 1997, pp. 170-170
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Citation: Pm. Hagg et al., CLONING OF MOUSE TYPE-XV COLLAGEN SEQUENCES AND MAPPING OF THE CORRESPONDING GENE TO 4B1-3 - COMPARISON OF MOUSE AND HUMAN ALPHA-1(XV) COLLAGEN SEQUENCES INDICATES DIVERGENCE IN THE NUMBER OF SMALL COLLAGENOUSDOMAINS, Genomics, 45(1), 1997, pp. 31-41
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Citation: P. Koivunen et al., STRUCTURES OF THE HUMAN GENE FOR THE PROTEIN DISULFIDE ISOMERASE-RELATED POLYPEPTIDE ERP60 AND A PROCESSED GENE AND ASSIGNMENT OF THESE GENES TO 15Q15 AND 1Q21, Genomics, 42(3), 1997, pp. 397-404
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Citation: J. Kaukonen et al., THE MAPPING AND VISUAL ORDERING OF THE HUMAN SYNDECAN-1 AND N-MYC GENES NEAR THE TELOMERIC REGION OF CHROMOSOME 2P, Human genetics, 99(3), 1997, pp. 295-297
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Citation: T. Lauteala et al., HUMAN CATIONIC AMINO-ACID TRANSPORTER GENE HCAT-2 IS ASSIGNED TO 8P22BUT IS NOT THE CAUSATIVE GENE IN LYSINURIC PROTEIN INTOLERANCE, Human genetics, 100(1), 1997, pp. 80-83
Citation: J. Sinisalo et al., LOW-FREQUENCY OF FV R506G MUTATION IN A FINNISH VENOUS THROMBOSIS POPULATION, Thrombosis and haemostasis, 1997, pp. 918-918
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Citation: H. Mikkola et al., MOLECULAR-GENETICS OF FXIII DEFICIENCY IN EUROPE, Thrombosis and haemostasis, 1997, pp. 1553-1553
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Citation: U. Wartiovaara et al., VASCULAR ENDOTHELIAL GROWTH-FACTOR-C (VEGF-C) IS EXPRESSED IN THROMBOCYTES, Thrombosis and haemostasis, 1997, pp. 3018-3018
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Citation: H. Mikkola et al., MOLECULAR MECHANISMS OF MUTATIONS IN FACTOR-XIII A-SUBUNIT DEFICIENCY- IN-VITRO EXPRESSION IN COS-CELLS DEMONSTRATES INTRACELLULAR DEGRADATION OF THE MUTANT PROTEINS, Thrombosis and haemostasis, 77(6), 1997, pp. 1068-1072
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