Dorval I - Search Results

1

French CF family genotype analysis shows that the R297Q mutation is a rare polymorphism.

Dorval I, Jézéquel P, Chauvel B, Dubourg C, Fergelot P, Le Gall JY, Roussey M, Blayau M. Dorval I, et al. Hum Mutat. 1995;6(4):334-5. doi: 10.1002/humu.1380060407. Hum Mutat. 1995. PMID: 8680407

2

Structural analysis of CFTR gene in congenital bilateral absence of vas deferens.

Jézéquel P, Dorval I, Fergelot P, Chauvel B, Le Treut A, Le Gall JY, Le Lannou D, Blayau M. Jézéquel P, et al. Among authors: dorval i. Clin Chem. 1995 Jun;41(6 Pt 1):833-5. Clin Chem. 1995. PMID: 7539342

3

Obstructive azoospermia with agenesis of vas deferens or with bronchiectasia (Young's syndrome): a genetic approach.

Le Lannou D, Jezequel P, Blayau M, Dorval I, Lemoine P, Dabadie A, Roussey M, Le Marec B, Legall JY. Le Lannou D, et al. Among authors: dorval i. Hum Reprod. 1995 Feb;10(2):338-41. doi: 10.1093/oxfordjournals.humrep.a135939. Hum Reprod. 1995. PMID: 7539448

4

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. Hum Genet. 1993 Apr;91(3):254-6. doi: 10.1007/BF00218266. Hum Genet. 1993. PMID: 8097485

5

Allele frequencies of hereditary hemochromatosis gene mutations in a local population of west Brittany.

Jézéquel P, Bargain M, Lellouche F, Geffroy F, Dorval I. Jézéquel P, et al. Among authors: dorval i. Hum Genet. 1998 Mar;102(3):332-3. doi: 10.1007/s004390050701. Hum Genet. 1998. PMID: 9544848

6

Rapid detection of 1078 delT mutation by PCR-mediated site-directed mutagenesis: detection of cystic fibrosis carriers in a celtic population.

Dorval I, Fergelot P, Dubourg C, Jézéquel P, Chauvel B, Le Gall JY, Le Treut A. Dorval I, et al. Clin Chem. 1994 Dec;40(12):2318-9. Clin Chem. 1994. PMID: 7527310 No abstract available.

7

Identification of the homozygous missense mutation in the lecithin:cholesterol-acyltransferase (LCAT) gene, causing LCAT familial deficiency in two French patients.

Dorval I, Jezequel P, Dubourg C, Chauvel B, Le Pogamp P, Le Gall JY. Dorval I, et al. Atherosclerosis. 1994 Feb;105(2):251-2. doi: 10.1016/0021-9150(94)90056-6. Atherosclerosis. 1994. PMID: 8003101 No abstract available.

8

[Molecular genetics of hemochromatosis].

Le Gall JY, David V, Yaouanq J, Périchon M, Blayau M, Jouanolle AM, Mauvieux V, el Kahloun A, Chauvel B, Dorval I, et al. Le Gall JY, et al. Among authors: dorval i. Bull Acad Natl Med. 1993 Feb;177(2):187-98; discussion 199-201. Bull Acad Natl Med. 1993. PMID: 8353773 Review. French.

9

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: dorval i. Hum Mol Genet. 1993 Jan;2(1):55-60. doi: 10.1093/hmg/2.1.55. Hum Mol Genet. 1993. PMID: 8490624

10

Proteases.

Nduwimana J, Guenet L, Dorval I, Blayau M, Le Gall JY, Le Treut A. Nduwimana J, et al. Among authors: dorval i. Ann Biol Clin (Paris). 1995;53(5):251-64. Ann Biol Clin (Paris). 1995. PMID: 7574113 Review.

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