David V - Search Results

1

Identification of three novel mutations in the dystrophin gene detected by the heteroduplex/SSCA screening procedure. Mutations in brief no. 222. Online.

Dubourg C, Odent S, Fergelot P, Le Gall JY, David V, Blayau M. Dubourg C, et al. Among authors: david v. Hum Mutat. 1999;13(2):173. doi: 10.1002/(SICI)1098-1004(1999)13:2<173::AID-HUMU20>3.0.CO;2-3. Hum Mutat. 1999. PMID: 10094565

2

Analysis of 160 CF chromosomes: detection of a novel mutation in exon 20.

Dorval I, Odent S, Jezequel P, Journel H, Chauvel B, Dabadie A, Roussey M, Le Gall JY, Le Marec B, David V, et al. Dorval I, et al. Among authors: david v. Hum Genet. 1993 Apr;91(3):254-6. doi: 10.1007/BF00218266. Hum Genet. 1993. PMID: 8097485

3

Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutations.

Jézéquel P, Dubourg C, Le Lannou D, Odent S, Le Gall JY, Blayau M, Le Treut A, David V. Jézéquel P, et al. Among authors: david v. Mol Hum Reprod. 2000 Dec;6(12):1063-7. doi: 10.1093/molehr/6.12.1063. Mol Hum Reprod. 2000. PMID: 11101688

4

Dinucleotide repeat polymorphism at the FTHPI locus of chromosome 6.

Mauvieux V, Jouanolle AM, el Kahloun A, Blayau M, Le Gall JY, David V. Mauvieux V, et al. Among authors: david v. Nucleic Acids Res. 1991 Dec 25;19(24):6969. doi: 10.1093/nar/19.24.6969. Nucleic Acids Res. 1991. PMID: 1762936 Free PMC article.

5

HLA class I gene polymorphism in genetic hemochromatosis.

Jouanolle AM, Yaouanq J, Blayau M, Périchon M, Fauchet R, Font MP, Le Gall JY, David V. Jouanolle AM, et al. Among authors: david v. Hum Genet. 1990 Aug;85(3):279-82. doi: 10.1007/BF00206746. Hum Genet. 1990. PMID: 1975556

6

Ferritin H gene polymorphism in idiopathic hemochromatosis.

David V, Papadopoulos P, Yaouanq J, Blayau M, Abel L, Zappone E, Perichon M, Drysdale J, Le Gall JY, Simon M. David V, et al. Hum Genet. 1989 Jan;81(2):123-6. doi: 10.1007/BF00293887. Hum Genet. 1989. PMID: 2563249

7

Dinucleotide repeat polymorphism at the D6S510 locus.

Gandon G, Lelaure V, Pichon L, Jouanolle AM, Le Gall JY, David V. Gandon G, et al. Among authors: david v. Hum Mol Genet. 1994 Jul;3(7):1210. doi: 10.1093/hmg/3.7.1210. Hum Mol Genet. 1994. PMID: 7981708 No abstract available.

8

Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE).

Gandon G, Jouanolle AM, Chauvel B, Mauvieux V, le Treut A, Feingold J, Le Gall JY, David V, Yaouanq J. Gandon G, et al. Among authors: david v. Hum Genet. 1996 Jan;97(1):103-13. doi: 10.1007/BF00218843. Hum Genet. 1996. PMID: 8557248

9

[Genetic hemochromatosis].

Jouanolle AM, David V, Le Gall JY. Jouanolle AM, et al. Among authors: david v. Ann Biol Clin (Paris). 1997 May-Jun;55(3):189-93. Ann Biol Clin (Paris). 1997. PMID: 9238420 Free article. Review. French.

10

A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.

Jouanolle AM, Fergelot P, Gandon G, Yaouanq J, Le Gall JY, David V. Jouanolle AM, et al. Among authors: david v. Hum Genet. 1997 Oct;100(5-6):544-7. doi: 10.1007/s004390050549. Hum Genet. 1997. PMID: 9341868

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