AAAAAA

   
Results: 1-13 |
Results: 13
MOLECULAR-BASIS OF VASCULAR ANOMALIES
Authors: VIKKULA M BOON LM MULLIKEN JB OLSEN BR
Citation: M. Vikkula et al., MOLECULAR-BASIS OF VASCULAR ANOMALIES, Trends in cardiovascular medicine, 8(7), 1998, pp. 281-292
THE GENE RESPONSIBLE FOR PSEUDOHYPOPARATHYROIDISM TYPE IB IS PATERNALLY IMPRINTED AND MAPS IN 4 UNRELATED KINDREDS TO CHROMOSOME 20Q13.3
Authors: JUPPNER H SCHIPANI E BASTEPE M COLE DEC LAWSON ML MANNSTADT M HENDY GN PLOTKIN H KOSHIYAMA H KOH T CRAWFORD JD OLSEN BR VIKKULA M
Citation: H. Juppner et al., THE GENE RESPONSIBLE FOR PSEUDOHYPOPARATHYROIDISM TYPE IB IS PATERNALLY IMPRINTED AND MAPS IN 4 UNRELATED KINDREDS TO CHROMOSOME 20Q13.3, Proceedings of the National Academy of Sciences of the United Statesof America, 95(20), 1998, pp. 11798-11803
A GENE ON CHROMOSOME 11Q23 CODING FOR A PUTATIVE GLUCOSE-6-PHOSPHATE TRANSLOCASE IS MUTATED IN GLYCOGEN-STORAGE-DISEASE TYPES IB AND IC
Authors: VEIGADACUNHA M GERIN I CHEN YT DEBARSY T DELONLAY P DIONISIVICI C FENSKE CD LEE PJ LEONARD JV MAIRE I MCCONKIEROSELL A SCHWEITZER S VIKKULA M VANSCHAFTINGEN E
Citation: M. Veigadacunha et al., A GENE ON CHROMOSOME 11Q23 CODING FOR A PUTATIVE GLUCOSE-6-PHOSPHATE TRANSLOCASE IS MUTATED IN GLYCOGEN-STORAGE-DISEASE TYPES IB AND IC, American journal of human genetics, 63(4), 1998, pp. 976-983
MOLECULAR BACKGROUND OF CONGENITAL VENOUS MALFORMATIONS
Authors: VIKKULA M BOON LM ZHUANG Z WARMAN ML LIOTTA L MULLIKEN JB OLSEN BR
Citation: M. Vikkula et al., MOLECULAR BACKGROUND OF CONGENITAL VENOUS MALFORMATIONS, American journal of human genetics, 61(4), 1997, pp. 51-51
UNRAVELING THE MOLECULAR-GENETICS OF OSTEOARTHROSIS
Authors: VIKKULA M OLSEN BR
Citation: M. Vikkula et Br. Olsen, UNRAVELING THE MOLECULAR-GENETICS OF OSTEOARTHROSIS, Annals of medicine, 28(4), 1996, pp. 301-304
VASCULAR DYSMORPHOGENESIS CAUSED BY AN ACTIVATING MUTATION IN THE RECEPTOR TYROSINE KINASE TIE2
Authors: VIKKULA M BOON LM CARRAWAY KL CALVERT JT DIAMONTI AJ GOUMNEROV B PASYK KA MARCHUK DA WARMAN ML CANTLEY LC MULLIKEN JB OLSEN BR
Citation: M. Vikkula et al., VASCULAR DYSMORPHOGENESIS CAUSED BY AN ACTIVATING MUTATION IN THE RECEPTOR TYROSINE KINASE TIE2, Cell, 87(7), 1996, pp. 1181-1190
OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME, A DISORDER AFFECTING SKELETAL STRENGTH AND VISION, IS ASSIGNED TO CHROMOSOME REGION 11Q12-13
Authors: GONG YQ VIKKULA M BOON L LIU J BEIGHTON P RAMESAR R PELTONEN L SOMER H HIROSE T DALLAPICCOLA B DEPAEPE A SWOBODA W ZABEL B SUPERTIFURGA A STEINMANN B BRUNNER HG JANS A BOLES RG ADKINS W VANDENBOOGAARD MJ OLSEN BR WARMAN ML
Citation: Yq. Gong et al., OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME, A DISORDER AFFECTING SKELETAL STRENGTH AND VISION, IS ASSIGNED TO CHROMOSOME REGION 11Q12-13, American journal of human genetics, 59(1), 1996, pp. 146-151
AUTOSOMAL-DOMINANT AND RECESSIVE OSTEOCHONDRODYSPLASIAS ASSOCIATED WITH THE COL11A2 LOCUS
Authors: VIKKULA M MARIMAN ECM LUI VCH ZHIDKOVA NI TILLER GE GOLDRING MB VANBEERSUM SEC MALEFIJT MCD VANDENHOOGEN FHJ ROPERS HH MAYNE R CHEAH KSE OLSEN BR WARMAN ML BRUNNER HG
Citation: M. Vikkula et al., AUTOSOMAL-DOMINANT AND RECESSIVE OSTEOCHONDRODYSPLASIAS ASSOCIATED WITH THE COL11A2 LOCUS, Cell, 80(3), 1995, pp. 431-437
A GENE FOR FAMILIAL VENOUS MALFORMATIONS MAPS TO CHROMOSOME-9P IN A 2ND LARGE KINDRED
Authors: GALLIONE CJ PASYK KA BOON LM LENNON F JOHNSON DW HELMBOLD EA MARKEL DS VIKKULA M MULLIKEN JB WARMAN ML PERICAKVANCE MA MARCHUK DA
Citation: Cj. Gallione et al., A GENE FOR FAMILIAL VENOUS MALFORMATIONS MAPS TO CHROMOSOME-9P IN A 2ND LARGE KINDRED, Journal of Medical Genetics, 32(3), 1995, pp. 197-199
IDENTIFICATION OF COL2A1 GENE-MUTATIONS IN PATIENTS WITH CHONDRODYSPLASIAS AND FAMILIAL OSTEOARTHRITIS
Authors: RITVANIEMI P KORKKO J BONAVENTURE J VIKKULA M HYLAND J PAASSILTA P KAITILA I KAARIAINEN H SOKOLOV BP HAKALA M MANNISMAKI P MEERSON EM KLEMOLA T WILLIAMS C PELTONEN L KIVIRIKKO KI PROCKOP DJ ALAKOKKO L
Citation: P. Ritvaniemi et al., IDENTIFICATION OF COL2A1 GENE-MUTATIONS IN PATIENTS WITH CHONDRODYSPLASIAS AND FAMILIAL OSTEOARTHRITIS, Arthritis and rheumatism, 38(7), 1995, pp. 999-1004
ASSIGNMENT OF A LOCUS FOR DOMINANTLY INHERITED VENOUS MALFORMATIONS TO CHROMOSOME 9P
Authors: BOON LM MULLIKEN JB VIKKULA M WATKINS H SEIDMAN J OLSEN BR WARMAN ML
Citation: Lm. Boon et al., ASSIGNMENT OF A LOCUS FOR DOMINANTLY INHERITED VENOUS MALFORMATIONS TO CHROMOSOME 9P, Human molecular genetics, 3(9), 1994, pp. 1583-1587
TYPE-II COLLAGEN MUTATIONS IN RARE AND COMMON CARTILAGE DISEASES
Authors: VIKKULA M METSARANTA M ALAKOKKO L
Citation: M. Vikkula et al., TYPE-II COLLAGEN MUTATIONS IN RARE AND COMMON CARTILAGE DISEASES, Annals of medicine, 26(2), 1994, pp. 107-114
MULTIALLELIC POLYMORPHISM OF THE CARTILAGE COLLAGEN GENE - NO ASSOCIATION WITH OSTEOARTHROSIS
Authors: VIKKULA M NISSILA M HIRVENSALO E NUOTIO P PALOTIE A AHO K PELTONEN L
Citation: M. Vikkula et al., MULTIALLELIC POLYMORPHISM OF THE CARTILAGE COLLAGEN GENE - NO ASSOCIATION WITH OSTEOARTHROSIS, Annals of the Rheumatic Diseases, 52(10), 1993, pp. 762-764
Risultati: 1-13 |