Authors:
CHUANG LM
WU HP
JANG MH
WANG TR
SUE WC
LIN BJ
COX DW
TAI TY
Citation: Lm. Chuang et al., HIGH-FREQUENCY OF 2 MUTATIONS IN CODON-778 IN EXON-8 OF THE ATP7B GENE IN TAIWANESE FAMILIES WITH WILSON-DISEASE, Journal of Medical Genetics, 33(6), 1996, pp. 521-523
Authors:
VEIJOLA R
KNIP M
PUUKKA R
REIJONEN H
COX DW
ILONEN J
Citation: R. Veijola et al., THE IMMUNOGLOBULIN HEAVY-CHAIN VARIABLE REGION IN INSULIN-DEPENDENT DIABETES-MELLITUS - AFFECTED-SIB-PAIR ANALYSIS AND ASSOCIATION STUDIES, American journal of human genetics, 59(2), 1996, pp. 462-470
Authors:
THOMAS GR
FORBES JR
ROBERTS EA
WALSHE JM
COX DW
Citation: Gr. Thomas et al., THE WILSON-DISEASE GENE - SPECTRUM OF MUTATIONS AND THEIR CONSEQUENCES, (VOL 9, PG 210, 1995), Nature genetics, 9(4), 1995, pp. 451-451
Authors:
CHALMERS RW
VAUGHAN PR
COATS DJ
MACDONALD A
DAWSON GM
COLESHILL DC
PONTIN JMA
COX DW
REID JM
ROCKE G
Citation: Rw. Chalmers et al., RECONSTRUCTED CARSINGTON-DAM - DESIGN AND PERFORMANCE, AND CONSTRUCTION - DISCUSSION, Proceedings of the Institution of Civil Engineers. Water, maritime and energy, 112(4), 1995, pp. 375-380
Citation: Dw. Cox et al., THE COPPER-BINDING ATPASE DEFECTIVE IN WILSON DISEASE - FUNCTIONAL INFORMATION FROM MUTATIONS, Journal of cellular biochemistry, 1995, pp. 241-241
Authors:
COX DW
GEDDEDAHL T
MENON AG
NYGAARD TG
TOMLINSON IM
PETERS J
STGEORGEHYSLOP PH
Citation: Dw. Cox et al., REPORT OF THE 2ND INTERNATIONAL WORKSHOP ON HUMAN-CHROMOSOME-14 MAPPING 1994, Cytogenetics and cell genetics, 69(3-4), 1995, pp. 160-171
Citation: Zq. Chen et al., DEFINING THE BREAKPOINT OF A MULTIGENE DELETION IN THE IMMUNOGLOBULINHEAVY-CHAIN GENE-CLUSTER, Immunogenetics, 41(2-3), 1995, pp. 69-73
Authors:
BYTH BC
COSTA MT
TESHIMA IE
WILSON WG
CARTER NP
COX DW
Citation: Bc. Byth et al., MOLECULAR ANALYSIS OF 3 PATIENTS WITH INTERSTITIAL DELETIONS OF CHROMOSOME BAND 14Q31, Journal of Medical Genetics, 32(7), 1995, pp. 564-567
Authors:
LOMAS DA
ELLIOTT PR
SIDHAR SK
FOREMAN RC
FINCH JT
COX DW
WHISSTOCK JC
CARRELL RW
Citation: Da. Lomas et al., ALPHA(1)-ANTITRYPSIN MMALTON (PHE(52)-DELETED) FORMS LOOP-SHEET POLYMERS IN-VIVO - EVIDENCE FOR THE C-SHEET MECHANISM OF POLYMERIZATION, The Journal of biological chemistry, 270(28), 1995, pp. 16864-16870
Authors:
PENMAN ADM
COX DW
KENNARD MF
BROMHEAD EN
DUNSTER JA
ROWE PW
TAYLOR EH
Citation: Adm. Penman et al., THE FAILURE OF CARSINGTON-DAM - INVESTIGATION OF THE FAILURE OF CARSINGTON-DAM - DISCUSSION, Geotechnique, 45(4), 1995, pp. 719-739
Authors:
PLODER L
LIU L
DECHEN J
DUNCAN A
NGUYEN V
COX DW
TRABOULSI E
LEVIN A
MCINNES RR
Citation: L. Ploder et al., CLONING OF THE HUMAN CHX10 GENE AND MUTATION SCREENING OF CANDIDATE DISEASE, American journal of human genetics, 57(4), 1995, pp. 772-772
Citation: Rf. Wintle et al., PHYSICAL AND GENETIC-ANALYSIS OF A SUBTELOMERIC REGION FROM HUMAN-CHROMOSOME-14, CONTAINING THE IMMUNOGLOBULIN HEAVY-CHAIN GENE-CLUSTER, American journal of human genetics, 57(4), 1995, pp. 1184-1184
Authors:
NGUYEN VTT
BYTH BC
CONNELLY PW
HEGELE RA
COX DW
Citation: Vtt. Nguyen et al., KALLISTATIN - MAPPING IN THE SERPIN CLUSTER AT 14Q32.1 AND POTENTIAL ASSOCIATION WITH HYPERTENSION, American journal of human genetics, 57(4), 1995, pp. 1850-1850
Citation: Js. Wu et al., THE LEC RAT HAS A DELETION IN THE COPPER TRANSPORTING ATPASE GENE HOMOLOGOUS TO THE WILSON DISEASE GENE, Nature genetics, 7(4), 1994, pp. 541-545
Authors:
BULL PC
THOMAS GR
ROMMENS JM
FORBES JR
COX DW
Citation: Pc. Bull et al., THE WILSON DISEASE GENE IS A PUTATIVE COPPER TRANSPORTING P-TYPE ATPASE SIMILAR TO THE MENKES GENE (VOL 5, PG 327, 1993), Nature genetics, 6(2), 1994, pp. 214-214