Fujiwara TM - Search Results

1

Cystic fibrosis mutations in the Hutterite Brethren.

Klinger K, Horn GT, Stanislovitis P, Schwartz RH, Fujiwara TM, Morgan K. Klinger K, et al. Among authors: fujiwara tm. Am J Hum Genet. 1990 May;46(5):983-7. Am J Hum Genet. 1990. PMID: 2339696 Free PMC article.

2

Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren.

Fujiwara TM, Morgan K, Schwartz RH, Doherty RA, Miller SR, Klinger K, Stanislovitis P, Stuart N, Watkins PC. Fujiwara TM, et al. Am J Hum Genet. 1989 Mar;44(3):327-37. Am J Hum Genet. 1989. PMID: 2563632 Free PMC article.

3

Identification of the M1101K mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and complete detection of cystic fibrosis mutations in the Hutterite population.

Zielenski J, Fujiwara TM, Markiewicz D, Paradis AJ, Anacleto AI, Richards B, Schwartz RH, Klinger KW, Tsui LC, Morgan K. Zielenski J, et al. Among authors: fujiwara tm. Am J Hum Genet. 1993 Mar;52(3):609-15. Am J Hum Genet. 1993. PMID: 7680525 Free PMC article.

4

Cystic fibrosis mutations in French Canadians: three CFTR mutations are relatively frequent in a Quebec population with an elevated incidence of cystic fibrosis.

Rozen R, De Braekeleer M, Daigneault J, Ferreira-Rajabi L, Gerdes M, Lamoureux L, Aubin G, Simard F, Fujiwara TM, Morgan K. Rozen R, et al. Among authors: fujiwara tm. Am J Med Genet. 1992 Feb 1;42(3):360-4. doi: 10.1002/ajmg.1320420322. Am J Med Genet. 1992. PMID: 1536179

5

Dental agenesis in the Dariusleut Hutterite Brethren: comparisons to selected Caucasoid population surveys.

Mahaney MC, Fujiwara TM, Morgan K. Mahaney MC, et al. Among authors: fujiwara tm. Am J Phys Anthropol. 1990 Jun;82(2):165-77. doi: 10.1002/ajpa.1330820205. Am J Phys Anthropol. 1990. PMID: 2360610

6

X-linked hypophosphatemia: the mutant gene is expressed in teeth as well as in kidney.

Shields ED, Scriver CR, Reade T, Fujiwara TM, Morgan K, Ciampi A, Schwartz S. Shields ED, et al. Among authors: fujiwara tm. Am J Hum Genet. 1990 Mar;46(3):434-42. Am J Hum Genet. 1990. PMID: 2155529 Free PMC article.

7

Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene.

Frosk P, Weiler T, Nylen E, Sudha T, Greenberg CR, Morgan K, Fujiwara TM, Wrogemann K. Frosk P, et al. Among authors: fujiwara tm. Am J Hum Genet. 2002 Mar;70(3):663-72. doi: 10.1086/339083. Epub 2002 Jan 29. Am J Hum Genet. 2002. PMID: 11822024 Free PMC article.

8

Identification of deletion and triple alpha-globin gene haplotypes in the Montreal beta-thalassemia screening program: implications for genetic medicine.

Akerman BR, Fujiwara TM, Lancaster GA, Morgan K, Scriver CR. Akerman BR, et al. Among authors: fujiwara tm. Am J Med Genet. 1990 May;36(1):76-84. doi: 10.1002/ajmg.1320360115. Am J Med Genet. 1990. PMID: 2333910

9

Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family.

Greenwood CM, Fujiwara TM, Boothroyd LJ, Miller MA, Frappier D, Fanning EA, Schurr E, Morgan K. Greenwood CM, et al. Among authors: fujiwara tm. Am J Hum Genet. 2000 Aug;67(2):405-16. doi: 10.1086/303012. Epub 2000 Jul 5. Am J Hum Genet. 2000. PMID: 10882571 Free PMC article.

10

Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.

Goobie S, Popovic M, Morrison J, Ellis L, Ginzberg H, Boocock GR, Ehtesham N, Bétard C, Brewer CG, Roslin NM, Hudson TJ, Morgan K, Fujiwara TM, Durie PR, Rommens JM. Goobie S, et al. Among authors: fujiwara tm. Am J Hum Genet. 2001 Apr;68(4):1048-54. doi: 10.1086/319505. Epub 2001 Mar 15. Am J Hum Genet. 2001. PMID: 11254457 Free PMC article.

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