Kaplan JC - Search Results

1

G6PD Aures: a new mutation (48 Ile-->Thr) causing mild G6PD deficiency is associated with favism.

Nafa K, Reghis A, Osmani N, Baghli L, Benabadji M, Kaplan JC, Vulliamy TJ, Luzzatto L. Nafa K, et al. Among authors: kaplan jc. Hum Mol Genet. 1993 Jan;2(1):81-2. doi: 10.1093/hmg/2.1.81. Hum Mol Genet. 1993. PMID: 8490627 No abstract available.

2

At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria.

Nafa K, Reghis A, Osmani N, Baghli L, Aït-Abbes H, Benabadji M, Kaplan JC, Vulliamy T, Luzzatto L. Nafa K, et al. Among authors: kaplan jc. Hum Genet. 1994 Nov;94(5):513-7. doi: 10.1007/BF00211017. Hum Genet. 1994. PMID: 7959686

3

Investigation of factor VIII:C gene restriction fragment length polymorphisms and search for deletions in hemophiliac subjects in Algeria.

Nafa K, Meriane F, Reghis A, Benabadji M, Demenais F, Guilloud-Bataille M, Sultan Y, Kaplan JC, Delpech M. Nafa K, et al. Among authors: kaplan jc. Hum Genet. 1990 Apr;84(5):401-5. doi: 10.1007/BF00195808. Hum Genet. 1990. PMID: 1969840

4

Screening for mutations in factor VIII gene using the single-strand conformation polymorphism.

Nafa K, Meriane F, Chellali T, Benabadji M, Reghis A, Viemont M, Kaplan JC, Delpech M. Nafa K, et al. Among authors: kaplan jc. Hum Mutat. 1995;5(4):357-9. doi: 10.1002/humu.1380050418. Hum Mutat. 1995. PMID: 7627196 No abstract available.

5

A novel mutation (Arg-->Leu in exon 18) in factor VIII gene responsible for moderate hemophilia A.

Nafa K, Baudis M, Deburgrave N, Bardin JM, Sultan Y, Kaplan JC, Delpech M. Nafa K, et al. Among authors: kaplan jc. Hum Mutat. 1992;1(1):77-8. doi: 10.1002/humu.1380010114. Hum Mutat. 1992. PMID: 1301194 No abstract available.

6

Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria. Study in Northern Algeria with description of five new variants.

Benabadji M, Merad F, Benmoussa M, Trabuchet G, Junien C, Dreyfus JC, Kaplan JC. Benabadji M, et al. Among authors: kaplan jc. Hum Genet. 1978 Jan 19;40(2):177-84. doi: 10.1007/BF00272298. Hum Genet. 1978. PMID: 624546

7

A new TaqI allele at DXS52 frequent in Algeria.

Nafa K, Reghis A, Benabadji M, Delpech M, Kaplan JC. Nafa K, et al. Among authors: kaplan jc. Nucleic Acids Res. 1989 Feb 11;17(3):1276. doi: 10.1093/nar/17.3.1276. Nucleic Acids Res. 1989. PMID: 2564185 Free PMC article. No abstract available.

8

Quantitative variations of red-cell cytochrome b5 reductase (NADH-methemoglobin-reductase) in the Algerian population: evidence for defective alleles.

Reghis A, Benabadji M, Tchen P, Kaplan JC. Reghis A, et al. Among authors: kaplan jc. Hum Genet. 1981;59(2):148-55. doi: 10.1007/BF00293065. Hum Genet. 1981. PMID: 7327574

9

Characterization of weak alleles at the DIA1 locus (Mustapha 1, Mustapha 2, and Mustapha 3) in the Algerian population.

Reghis A, Troungos C, Lostanlen D, Krishnamoorthy R, Kaplan JC. Reghis A, et al. Among authors: kaplan jc. Hum Genet. 1983;64(2):173-5. doi: 10.1007/BF00327119. Hum Genet. 1983. PMID: 6885054

10

A linkage and physical map of chromosome 22, and some applications to gene mapping.

Julier C, Lathrop GM, Reghis A, Szajnert MF, Lalouel JM, Kaplan JC. Julier C, et al. Among authors: kaplan jc. Am J Hum Genet. 1988 Feb;42(2):297-308. Am J Hum Genet. 1988. PMID: 2893546 Free PMC article.

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