Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein geneJING LIU; FUJIWARA, T. M; SCHURR, E et al.American journal of human genetics. 1995, Vol 56, Num 4, pp 845-853, issn 0002-9297Article

Large-scale cloning of human chromosome 2-specific yeast artificial chromosomes (YACs) using an interspersed repetitive sequences (IRS)-PCR approachJING LIU; STANTON, V. P; FUJIWARA, T. M et al.Genomics (San Diego, Calif.). 1995, Vol 26, Num 2, pp 178-191, issn 0888-7543Article

Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13-14LABUDA, M; FUJIWARA, T. M; ROSS, M. V et al.Journal of bone and mineral research (Print). 1992, Vol 7, Num 12, pp 1447-1453, issn 0884-0431Article

Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite BrethrenFUJIWARA, T. M; MORGAN, K; SCHWARTZ, R. H et al.American journal of human genetics. 1989, Vol 44, Num 3, pp 327-337, issn 0002-9297Article

Localisation of a gene for mucopolysaccharidosis IIIC to the pericentromeric region of chromosome 8AUSSEIL, J; LOREDO-OSTI, J. C; PSHEZHETSKY, A. V et al.Journal of medical genetics. 2004, Vol 41, Num 12, pp 941-944, issn 0022-2593, 4 p.Article

Low prevalence of psychoses among the hutterites, an isolated religious communityNIMGAONKAR, V. L; FUJIWARA, T. M; DUTTA, M et al.The American journal of psychiatry. 2000, Vol 157, Num 7, pp 1065-1070, issn 0002-953XArticle

Molecular analysis of X-linked nephrogenic diabetes insipidusFUJIWARA, T. M; MORGAN, K; BICHET, D. G et al.European journal of endocrinology. 1996, Vol 134, Num 6, pp 675-677, issn 0804-4643Article

Identification of deletion and triple α-globin gene haplotypes in the Montreal β-thalassemia screening program : implications for genetic medicineAKERMAN, B. R; FUJIWARA, T. M; LANCASTER, G. A et al.American journal of medical genetics. 1990, Vol 36, Num 1, pp 76-84, issn 0148-7299, 9 p.Article

Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22 : And identification of a shared haplotypeBETARD, C; RASQUIN-WEBER, A; FUJIWARA, T. M et al.American journal of human genetics. 2000, Vol 67, Num 1, pp 222-228, issn 0002-9297Article

Association of apolipoprotein ε4 allele and neuropathologic findings in patients with dementiaMARTINOLI, M.-G; TROJANOWSKI, J. Q; SCHMIDT, M. L et al.Acta neuropathologica. 1995, Vol 90, Num 3, pp 239-243, issn 0001-6322Article

Molecular biology of diabetes insipidusFUJIWARA, T. M; MORGAN, K; BICHET, D. G et al.Annual review of medicine. 1995, Vol 46, pp 331-343, issn 0066-4219Article

Nature and recurrence of AVPR2 mutations in X-linked nephrogenic diabetes insipidusBICHET, D. G; BIRNBAUMER, M; FISH, A et al.American journal of human genetics. 1994, Vol 55, Num 2, pp 278-286, issn 0002-9297Article

X-linked nephrogenic diabetes insipidus : from the sip hopewell to RFLP studiesBICHET, D. G; HENDY, G. N; HIRSCH, D. J et al.American journal of human genetics. 1992, Vol 51, Num 5, pp 1089-1102, issn 0002-9297Article

Report of 33 novel AVPR2 mutations and analysis of 117 families with X-linked nephrogenic diabetes insipidusARTHUS, M.-F; LONERGAN, M; BICHET, D. G et al.Journal of the American Society of Nephrology. 2000, Vol 11, Num 6, pp 1044-1054, issn 1046-6673Article

Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD lociWEILER, T; GREENBERG, C. R; WROGEMANN, K et al.American journal of medical genetics. 1997, Vol 72, Num 3, pp 363-368, issn 0148-7299Article

X-linked nephrogenic diabetes insipidus mutations in North America and the Hopewell hypothesisBICHET, D. G; ARTHUS, M.-F; ANTARAMIAN, A et al.The Journal of clinical investigation. 1993, Vol 92, Num 3, pp 1262-1268, issn 0021-9738Article

Cystic fibrosis mutations in french canadians : three CFTR mutations are relatively frequent in a Quebec population with an elevated incidence of cystic fibrosisROZEN, R; DE BRAEKELEER, M; DAIGNEAULT, J et al.American journal of medical genetics. 1992, Vol 42, Num 3, pp 360-364, issn 0148-7299Article

Cystic fibrosis mutations in North American populations of french ancestry : analysis of Quebec French-Canadian and Louisiana Acadian familiesROZEN, R; SCHWARTZ, R. H; FUJIWARA, T. M et al.American journal of human genetics. 1990, Vol 47, Num 4, pp 606-610, issn 0002-9297, 5 p.Article

Cystic fibrosis mutation in the hutterite brethrenKLINGER, K; HORN, G. T; STANISLOVITIS, P et al.American journal of human genetics. 1990, Vol 46, Num 5, pp 983-987, issn 0002-9297, 5 p.Article

X-linked hypophosphatemia: the mutant gene is expressed in teeth as well as in kidneySHIELDS, E. D; SCRIVER, C. R; READE, T et al.American journal of human genetics. 1990, Vol 46, Num 3, pp 434-442, issn 0002-9297, 9 p.Article