David V - Search Results

1

Non-hyperfunctioning nodules from multinodular goiters: a minor role in pathogenesis for somatic activating mutations in the TSH-receptor and Gsalpha subunit genes.

Derrien C, Sonnet E, Gicquel I, Le Gall JY, Poirier JY, David V, Maugendre D. Derrien C, et al. Among authors: david v. J Endocrinol Invest. 2001 May;24(5):321-5. doi: 10.1007/BF03343868. J Endocrinol Invest. 2001. PMID: 11407651

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 genetics of hemochromatosis].

David V, Jouanolle AM, Fergelot P, Brissot P, Deugnier Y, Le Gall JY. David V, et al. Ann Endocrinol (Paris). 1999 Sep;60(3):204-9. Ann Endocrinol (Paris). 1999. PMID: 10520411 Review. French.

4

Localization of seven new genes around the HLA-A locus.

el Kahloun A, Chauvel B, Mauvieux V, Dorval I, Jouanolle AM, Gicquel I, le Gall JY, David V. el Kahloun A, et al. Among authors: david v. Adv Exp Med Biol. 1994;356:319-30. doi: 10.1007/978-1-4615-2554-7_34. Adv Exp Med Biol. 1994. PMID: 7887238 No abstract available.

5

Localization of seven new genes around the HLA-A locus.

el Kahloun A, Chauvel B, Mauvieux V, Dorval I, Jouanolle AM, Gicquel I, Le Gall JY, David V. el Kahloun A, et al. Among authors: david v. Hum Mol Genet. 1993 Jan;2(1):55-60. doi: 10.1093/hmg/2.1.55. Hum Mol Genet. 1993. PMID: 8490624

6

[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.

7

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

8

[Genetic hemochromatosis].

Jouanolle AM, Gandon G, Le Gall JY, David V. Jouanolle AM, et al. Among authors: david v. Ann Biol Clin (Paris). 1998 Jul;56 Spec No:31-5. Ann Biol Clin (Paris). 1998. PMID: 9827212 Review. French. No abstract available.

9

Polymorphisms in the HFE gene.

Douabin V, Moirand R, Jouanolle A, Brissot P, Le Gall J, Deugnier Y, David V. Douabin V, et al. Among authors: david v. Hum Hered. 1999 Jan;49(1):21-6. doi: 10.1159/000022835. Hum Hered. 1999. PMID: 9858853

10

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

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