De Meeus A - Search Results

1

Deciphering the molecular genetics of congenital heart disease.

Bouvagnet P, Sauer U, Debrus S, Genz T, Alonso S, Berger G, De Meeus A, Bühlmeier K, Demaille J. Bouvagnet P, et al. Among authors: de meeus a. Herz. 1994 Apr;19(2):119-25. Herz. 1994. PMID: 8194832 Review.

2

[Genetics of hereditary cardiopathies].

Debrus S, de Meeus A, Jean MK, Bouvagnet P. Debrus S, et al. Among authors: de meeus a. Arch Mal Coeur Vaiss. 1996 May;89(5):619-27. Arch Mal Coeur Vaiss. 1996. PMID: 8758572 Review. French.

3

[Mice SI/Col: a study model in the research of genes involved in situs inversus].

de Meeus A, Alonso S, Demaille J, Bouvagnet P. de Meeus A, et al. Arch Mal Coeur Vaiss. 1993 May;86(5):617-22. Arch Mal Coeur Vaiss. 1993. PMID: 8257272 French.

4

Familial non-syndromic conotruncal defects are not associated with a 22q11 microdeletion.

Debrus S, Berger G, de Meeus A, Sauer U, Guillaumont S, Voisin M, Bozio A, Demczuk S, Aurias A, Bouvagnet P. Debrus S, et al. Among authors: de meeus a. Hum Genet. 1996 Feb;97(2):138-44. doi: 10.1007/BF02265254. Hum Genet. 1996. PMID: 8566942

5

An isolated cardiac conduction disease maps to chromosome 19q.

de Meeus A, Stephan E, Debrus S, Jean MK, Loiselet J, Weissenbach J, Demaille J, Bouvagnet P. de Meeus A, et al. Circ Res. 1995 Oct;77(4):735-40. doi: 10.1161/01.res.77.4.735. Circ Res. 1995. PMID: 7554120

6

Blastogenesis dominant 1: a sequence with midline anomalies and heterotaxy.

de Meeus A, Sarda P, Tenconi R, Ferrière M, Bouvagnet P. de Meeus A, et al. Am J Med Genet. 1997 Feb 11;68(4):405-8. doi: 10.1002/(sici)1096-8628(19970211)68:4<405::aid-ajmg6>3.0.co;2-k. Am J Med Genet. 1997. PMID: 9021011

7

A detailed linkage map of subtelomeric murine chromosome 12 region including the situs inversus mutation locus IV.

de Meeus A, Alonso S, Demaille J, Bouvagnet P. de Meeus A, et al. Mamm Genome. 1992;3(11):637-43. doi: 10.1007/BF00352481. Mamm Genome. 1992. PMID: 1360279

8

Hereditary bundle branch defect: right bundle branch blocks of different causes have different morphologic characteristics.

Stéphan E, de Meeus A, Bouvagnet P. Stéphan E, et al. Among authors: de meeus a. Am Heart J. 1997 Feb;133(2):249-56. doi: 10.1016/s0002-8703(97)70215-1. Am Heart J. 1997. PMID: 9023172

9

Linkage disequilibrium between the M470V variant and the IVS8 polyT alleles of the CFTR gene in CBAVD.

de Meeus A, Guittard C, Desgeorges M, Carles S, Demaille J, Claustres M. de Meeus A, et al. J Med Genet. 1998 Jul;35(7):594-6. doi: 10.1136/jmg.35.7.594. J Med Genet. 1998. PMID: 9678705 Free PMC article.

10

Genetic findings in congenital bilateral aplasia of vas deferens patients and identification of six novel mutatations. Mutations in brief no. 138. Online.

de Meeus A, Guittard C, Desgeorges M, Carles S, Demaille J, Claustres M. de Meeus A, et al. Hum Mutat. 1998;11(6):480. doi: 10.1002/(SICI)1098-1004(1998)11:6<480::AID-HUMU9>3.0.CO;2-4. Hum Mutat. 1998. PMID: 10200050

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