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

Current status of human chromosome 14KAMNASARAN, D; COX, D. W.Journal of medical genetics. 2002, Vol 39, Num 2, pp 81-90, 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

Disorders of copper transportCOX, D. W.British medical bulletin. 1999, Vol 55, Num 3, pp 544-555, issn 0007-1420Article

Physical and transcription map in the region 14q24.3 : Identification of six novel transcriptsROUX, A.-F; ROMMENS, J. M; READ, L et al.Genomics (San Diego, Calif.). 1997, Vol 43, Num 2, pp 130-140, issn 0888-7543Article

High frequency of two mutations in codon 778 in exon 8 of the ATP7B gene in Taiwanese families with Wilson diseaseCHUANG, L.-M; WU, H.-P; JANG, M.-H et al.Journal of medical genetics. 1996, Vol 33, Num 6, pp 521-524, issn 0022-2593, 3 p.Article

Tandem repeats 3' of the IGHA genes in the human immunoglobulin heavy chain gene clusterKANG, H. K; COX, D. W.Genomics (San Diego, Calif.). 1996, Vol 35, Num 1, pp 189-195, issn 0888-7543Article

Immunoglobulin heavy chain variable region polymorphisms and multiple sclerosis susceptibilityHASHIMOTO, L. L; WALTER, M. A; COX, D. W et al.Journal of neuroimmunology. 1993, Vol 44, Num 1, pp 77-83, issn 0165-5728Article

A deletion map of the human immunoglobulin heavy chain variable regionWALTER, M. A; DOSCH, H. M; COX, D. W et al.The Journal of experimental medicine. 1991, Vol 174, Num 2, pp 335-349, issn 0022-1007Article

Isolation and regional localization of 25 anonymous DNA probes on a chromosome 13 hybrid panelHOUWEN, R. H. J; PAUTLER, S. E; BARWELL, J. A et al.Cytogenetics and cell genetics. 1991, Vol 57, Num 2-3, pp 87-90, issn 0301-0171Article

The physical organization of the human immunoglobulin heavy chain gene complexWALTER, M. A; SURTI, U; HOFKER, M. H et al.EMBO journal (Print). 1990, Vol 9, Num 10, pp 3303-3313, issn 0261-4189, 11 p.Article

Sacrospinous ligament fixation at the time of transvaginal hysterectomy. DiscussionCRUIKSHANK, S. H; COX, D. W; MORLEY, G. W et al.American journal of obstetrics and gynecology. 1990, Vol 162, Num 6, pp 1611-1619, issn 0002-9378, 9 p.Conference Paper

RsaI polymorphism of a human immunoglobulin VH5 subclass locusSAM, M; WALTER, M. A; COX, D. W et al.Nucleic acids research. 1988, Vol 16, Num 17, issn 0305-1048, 8748Article