Kaplan F - Search Results

1

Beta-thalassemia genes in French-Canadians: haplotype and mutation analysis of Portneuf chromosomes.

Kaplan F, Kokotsis G, DeBraekeleer M, Morgan K, Scriver CR. Kaplan F, et al. Am J Hum Genet. 1990 Jan;46(1):126-32. Am J Hum Genet. 1990. PMID: 1967205 Free PMC article.

2

The intron 7 donor splice site transition: a second Tay-Sachs disease mutation in French Canada.

Hechtman P, Boulay B, De Braekeleer M, Andermann E, Melançon S, Larochelle J, Prevost C, Kaplan F. Hechtman P, et al. Among authors: kaplan f. Hum Genet. 1992 Dec;90(4):402-6. doi: 10.1007/BF00220467. Hum Genet. 1992. PMID: 1483696

3

Quantitation of beta-thalassemia genes in Quebec immigrants of Mediterranean, southeast Asian, and Asian Indian origins.

Kaplan F, Kokotsis G, Capua A, Scriver CR. Kaplan F, et al. Clin Invest Med. 1991 Aug;14(4):325-30. Clin Invest Med. 1991. PMID: 1782730

4

More than one mutant allele causes infantile Tay-Sachs disease in French-Canadians.

Hechtman P, Kaplan F, Bayleran J, Boulay B, Andermann E, de Braekeleer M, Melançon S, Lambert M, Potier M, Gagné R, et al. Hechtman P, et al. Among authors: kaplan f. Am J Hum Genet. 1990 Nov;47(5):815-22. Am J Hum Genet. 1990. PMID: 2220821 Free PMC article.

5

Probable identity by descent and discovery of familial relationships by means of a rare beta-thalassemia haplotype.

Martino T, Kaplan F, Diamond S, Oppenheim A, Scriver CR. Martino T, et al. Among authors: kaplan f. Hum Mutat. 1997;9(1):86-7. doi: 10.1002/(SICI)1098-1004(1997)9:1<86::AID-HUMU20>3.0.CO;2-K. Hum Mutat. 1997. PMID: 8990020 No abstract available.

6

Novel Tay-Sachs disease mutations from China.

Akalin N, Shi HP, Vavougios G, Hechtman P, Lo W, Scriver CR, Mahuran D, Kaplan F. Akalin N, et al. Among authors: kaplan f. Hum Mutat. 1992;1(1):40-6. doi: 10.1002/humu.1380010107. Hum Mutat. 1992. PMID: 1301190

7

Specificity and sensitivity of hexosaminidase assays and DNA analysis for the detection of Tay-Sachs disease gene carriers among Ashkenazic Jews.

Fernandes MJ, Kaplan F, Clow CL, Hechtman P, Scriver CR. Fernandes MJ, et al. Among authors: kaplan f. Genet Epidemiol. 1992;9(3):169-75. doi: 10.1002/gepi.1370090303. Genet Epidemiol. 1992. PMID: 1387862

8

The French Canadian Tay-Sachs disease deletion mutation: identification of probable founders.

De Braekeleer M, Hechtman P, Andermann E, Kaplan F. De Braekeleer M, et al. Among authors: kaplan f. Hum Genet. 1992 Apr;89(1):83-7. doi: 10.1007/BF00207048. Hum Genet. 1992. PMID: 1577470

9

Cystic fibrosis carrier screening by DNA analysis: a pilot study of attitudes among participants.

Kaplan F, Clow C, Scriver CR. Kaplan F, et al. Am J Hum Genet. 1991 Jul;49(1):240-2. Am J Hum Genet. 1991. PMID: 2063873 Free PMC article. No abstract available.

10

A Pst+ polymorphism in the HEXA gene with an unusual geographic distribution.

Kaplan F, Kapoor S, Lee D, Fernandes M, Vienozinskis M, Mascisch A, Scriver CR, Lim-Steele J, Kaback M, Zeiger K, Zoossman-Diskin A, Bonne-Tamir B, Landels E, Bobrow M, Hechtman P. Kaplan F, et al. Eur J Hum Genet. 1993;1(4):301-5. doi: 10.1159/000472428. Eur J Hum Genet. 1993. PMID: 8081943

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