Emphysema of early onset associated with a complete deficiency of alpha-1-antitrypsin (null homozygotes)COX, D. W; LEVISON, H.The American review of respiratory disease. 1988, Vol 137, Num 2, pp 371-375, issn 0003-0805Article

Prenatal diagnosis of α₁ antitrypsin deficiency and estimates of fetal risk for diseaseCOX, D. W; MANSFIELD, T.Journal of medical genetics. 1987, Vol 24, Num 1, pp 52-59, issn 0022-2593Article

Genetic characterization and origin of Tunisian berbersCHAABANI, H; COX, D. W.Human heredity. 1988, Vol 38, Num 5, pp 308-316, issn 0001-5652, 9 p.Article

The copper chaperone Atox1 in canine copper toxicosis in Bedlington terriersNANJI, M. S; COX, D. W.Genomics (San Diego, Calif.). 1999, Vol 62, Num 1, pp 108-112, issn 0888-7543Article

Functional and antigenic concentrations of alpha-1-proteinase inhibitor after administration for the prevention of chronic lung disease of prematuritySTISKAL, J. A; ITO, S; COX, D. W et al.Biology of the neonate. 1999, Vol 76, Num 3, pp 134-143, issn 0006-3126Article

Molecular analysis redefines three human chromosome 14 deletionsWINTLE, R. F; COSTA, T; HASLAM, R. H. A et al.Human genetics. 1995, Vol 95, Num 5, pp 495-500, issn 0340-6717Article

Wilson disease in Iceland : a clinical and genetic studyTHOMAS, G. R; JENSSON, O; GUDMUNDSSON, G et al.American journal of human genetics. 1995, Vol 56, Num 5, pp 1140-1146, issn 0002-9297Article

CEPH consortium map of chromosome 14COX, D. W; BILLINGSLEY, G. D; WEISSENBACH, J et al.Cytogenetics and cell genetics. 1995, Vol 69, Num 3-4, pp 175-178, issn 0301-0171Article

Application of inverse PCR to isolation of end probes from cosmidsBYTH, B. C; THOMAS, G. R; HOFLAND, N et al.Nucleic acids research. 1994, Vol 22, Num 9, pp 1766-1767, issn 0305-1048Article

Localization and genetic linkage of the human immunoglobulin heavy chain genes and the creatine kinase brain (CKB) gene: identification of a hot spot for recombinationBENGER, J. C; TESHIMA, I; WALTER, M. A et al.Genomics (San Diego, Calif.). 1991, Vol 9, Num 4, pp 614-622, issn 0888-7543, 9 p.Article

Report of the committee on the genetic constitution of chromosome 14COX, D. W; NAKAMURA, Y; GEDDE-DAHL, T. JR et al.Cytogenetics and cell genetics. 1990, Vol 55, Num 1-4, pp 183-188, issn 0301-0171, 6 p.Conference Paper

Techniques for site investigation using trial pits = Les techniques d'études de site utilisant des excavations testCOX, D. W; DAWSON, A. R; HALL, J. W et al.Engineering geology special publication. 1986, Num 2, pp 185-192, issn 0267-9914Conference Paper

Cystic fibrosis: analysis of linkage of the disease locus to red cell and plasma protein markersTSUI, L. C; COX, D. W; MCALPINE, P. J et al.Cytogenetics and cell genetics. 1985, Vol 39, Num 3, pp 238-239, issn 0301-0171Article

X;14 translocation: an exception to the critical region hypothesis on the human X-chromosomeMARKOVIC, V. D; COX, D. W; WILKINSON, J et al.American journal of medical genetics. 1985, Vol 20, Num 1, pp 87-96, issn 0148-7299Article

COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiologyCORONADO, V. A; BONNEVILLE, J. A; NAZER, H et al.Clinical genetics. 2005, Vol 68, Num 6, pp 548-551, issn 0009-9163, 4 p.Article

Genetic mapping of the copper toxicosis locus in bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16VAN DE SLUIS, B. J. A; BREEN, M; WIJMENGA, C et al.Human molecular genetics (Print). 1999, Vol 8, Num 3, pp 501-507, issn 0964-6906Article

Effect of treatment of Wilson's disease on natural history of haemochromatosisWALSHE, J. M; COX, D. W.Lancet (British edition). 1998, Vol 352, Num 9122, pp 112-113, issn 0140-6736Article

Proteinase inhibitor therapy for the prevention of chronic lung disease of prematurity : A randomized, controlled trialSTISKAL, J. A; DUNN, M. S; SHENNAN, A. T et al.Pediatrics (Evanston). 1998, Vol 101, Num 1, pp 89-94, issn 0031-4005, 1Article

Wilson diseaseROBERTS, E. A; COX, D. W.Baillière's clinical gastroenterology. 1998, Vol 12, Num 2, pp 237-256, issn 0950-3528Article

The immunoglobulin heavy-chain variable region in insulin-dependent diabetes mellitus : Affected-sib-pair analysis and association studiesVEIJOLA, R; KNIP, M; PUUKKA, R et al.American journal of human genetics. 1996, Vol 59, Num 2, pp 462-470, issn 0002-9297Article

Mapping of the mouse homologue of the Wilson disease gene to mouse chromosome 8REED, V; WILLIAMSON, P; BULL, P. C et al.Genomics (San Diego, Calif.). 1995, Vol 28, Num 3, pp 573-575, issn 0888-7543Article

Molecular analysis of three patients with interstitial deletions of chromosome band 14q31BYTH, B. C; COSTA, M. T; TESHIMA, I. E et al.Journal of medical genetics. 1995, Vol 32, Num 7, pp 564-567, issn 0022-2593Article

A heat shock gene at 14q22: mapping and expressionROUX, A.-F; NGUYEN, V. T. T; SQUIRE, J. A et al.Human molecular genetics (Print). 1994, Vol 3, Num 10, pp 1819-1822, issn 0964-6906Article

Regional localization of loci on chromosome 14 using somatic cell hybridsBILLINGSLEY, G. D; COX, D. W; DUNCAN, A. M. V et al.Cytogenetics and cell genetics. 1994, Vol 66, Num 1, pp 33-38, issn 0301-0171Conference Paper

Long range restriction mapping of 13q14.3 focused on the Wilson disease regionBULL, P. C; COX, D. W.Genomics (San Diego, Calif.). 1993, Vol 16, Num 3, pp 593-598, issn 0888-7543Article