David A - Search Results

1

Smooth muscle tumors associated with X-linked Alport syndrome: carrier detection in females.

Dahan K, Heidet L, Zhou J, Mettler G, Leppig KA, Proesmans W, David A, Roussel B, Mongeau JG, Gould JM, et al. Dahan K, et al. Among authors: david a. Kidney Int. 1995 Dec;48(6):1900-6. doi: 10.1038/ki.1995.489. Kidney Int. 1995. PMID: 8587250 Free article.

2

Novel COL4A5/COL4A6 deletions and further characterization of the diffuse leiomyomatosis-Alport syndrome (DL-AS) locus define the DL critical region.

Heidet L, Cohen-Solal L, Boye E, Thorner P, Kemper MJ, David A, Larget Piet L, Zhou J, Flinter F, Zhang X, Gubler MC, Antignac C. Heidet L, et al. Among authors: david a. Cytogenet Cell Genet. 1997;78(3-4):240-6. doi: 10.1159/000134666. Cytogenet Cell Genet. 1997. PMID: 9465897

3

[Diffuse leiomyomatosis with genital involvement and Alport syndrome. Report of two cases].

Le Bras A, David A, Knipping M, Mensier A, Heidet L, Lopes P. Le Bras A, et al. Among authors: david a. J Gynecol Obstet Biol Reprod (Paris). 1998 Sep;27(5):523-8. J Gynecol Obstet Biol Reprod (Paris). 1998. PMID: 9791580 Free article. French.

4

16p11.2 Locus modulates response to satiety before the onset of obesity.

Maillard AM, Hippolyte L, Rodriguez-Herreros B, Chawner SJ, Dremmel D, Agüera Z, Fagundo AB, Pain A, Martin-Brevet S, Hilbert A, Kurz S, Etienne R, Draganski B, Jimenez-Murcia S, Männik K, Metspalu A, Reigo A, Isidor B, Le Caignec C, David A, Mignot C, Keren B; 16p11.2 European Consortium; van den Bree MB, Munsch S, Fernandez-Aranda F, Beckmann JS, Reymond A, Jacquemont S. Maillard AM, et al. Among authors: david a. Int J Obes (Lond). 2016 May;40(5):870-6. doi: 10.1038/ijo.2015.247. Epub 2015 Dec 1. Int J Obes (Lond). 2016. PMID: 26620891 Free article.

5

Genetic heterogeneity of Usher syndrome type 1 in French families.

Larget-Piet D, Gerber S, Bonneau D, Rozet JM, Marc S, Ghazi I, Dufier JL, David A, Bitoun P, Weissenbach J, et al. Larget-Piet D, et al. Among authors: david a. Genomics. 1994 May 1;21(1):138-43. doi: 10.1006/geno.1994.1235. Genomics. 1994. PMID: 8088781

6

Exclusion of linkage between D3S47 (C17) and ADRPII gene in two large families of moderate autosomal dominant retinitis pigmentosa: evidence for genetic heterogeneity.

Kaplan J, Guasconi G, Dufier JL, Michel-Awad A, David A, Munnich A, Frezal J. Kaplan J, et al. Among authors: david a. Ann Genet. 1990;33(3):152-4. Ann Genet. 1990. PMID: 2288459

7

A series of 38 novel germline and somatic mutations of NIPBL in Cornelia de Lange syndrome.

Nizon M, Henry M, Michot C, Baumann C, Bazin A, Bessières B, Blesson S, Cordier-Alex MP, David A, Delahaye-Duriez A, Delezoïde AL, Dieux-Coeslier A, Doco-Fenzy M, Faivre L, Goldenberg A, Layet V, Loget P, Marlin S, Martinovic J, Odent S, Pasquier L, Plessis G, Prieur F, Putoux A, Rio M, Testard H, Bonnefont JP, Cormier-Daire V. Nizon M, et al. Among authors: david a. Clin Genet. 2016 May;89(5):584-9. doi: 10.1111/cge.12720. Epub 2016 Feb 3. Clin Genet. 2016. PMID: 26701315 Free article.

8

Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus.

Edery P, Pelet A, Mulligan LM, Abel L, Attié T, Dow E, Bonneau D, David A, Flintoff W, Jan D, et al. Edery P, et al. Among authors: david a. J Med Genet. 1994 Aug;31(8):602-6. doi: 10.1136/jmg.31.8.602. J Med Genet. 1994. PMID: 7815416 Free PMC article.

9

Digito-reno-cerebral syndrome: confirmation of Eronen syndrome.

Le Merrer M, David A, Goutieres F, Briard ML. Le Merrer M, et al. Among authors: david a. Clin Genet. 1992 Oct;42(4):196-8. doi: 10.1111/j.1399-0004.1992.tb03236.x. Clin Genet. 1992. PMID: 1424243

10

Somatic mosaicism and compound heterozygosity in female hemophilia B.

Costa JM, Vidaud D, Laurendeau I, Vidaud M, Fressinaud E, Moisan JP, David A, Meyer D, Lavergne JM. Costa JM, et al. Among authors: david a. Blood. 2000 Aug 15;96(4):1585-7. Blood. 2000. PMID: 10942410 Free article.

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