A de Meeus - JoVE Visualize

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American Heart Journal|February 1, 1997

Hereditary bundle branch defect: right bundle branch blocks of different causes have different morphologic characteristicsE Stéphan, A de Meeus, P Bouvagnet

Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992

A detailed linkage map of subtelomeric murine chromosome 12 region including the situs inversus mutation locus IVA de Meeus, S Alonso, J Demaille, et al.

Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1993

[Mice SI/Col: a study model in the research of genes involved in situs inversus]A de Meeus, S Alonso, J Demaille, et al.

Acta Neurologica Belgica|September 1, 1978

[Ventriculo-cardiac derivation in late complications of hemispherectomy (author's transl)]J Achslogh, J P Boucquey, A de Meeus, et al.

Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1996

[Genetics of hereditary cardiopathies]S Debrus, A de Meeus, M K Jean, et al.

American Journal of Medical Genetics|February 11, 1997

Blastogenesis dominant 1: a sequence with midline anomalies and heterotaxyA de Meeus, P Sarda, R Tenconi, et al.

Neuroradiology|August 25, 1977

The management of anterior sacral meningocele with computed tomographyD Balériaux-Waha, M Osteaux, G Terwinghe, et al.

Journal of Medical Genetics|July 25, 1998

Linkage disequilibrium between the M470V variant and the IVS8 polyT alleles of the CFTR gene in CBAVDA de Meeus, C Guittard, M Desgeorges, et al.

Human Mutation|April 13, 1999

Genetic findings in congenital bilateral aplasia of vas deferens patients and identification of six novel mutatations. Mutations in brief no. 138. OnlineA de Meeus, C Guittard, M Desgeorges, et al.

Journal Francais D'Ophtalmologie|October 6, 1998

[Clinical features and genetic analysis in a family with X-linked incomplete congenital stationary night blindness (CSNBi)]C F Schmitt-Bernard, C Bareil, C P Hamel, et al.

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Showing results (1-10 of 13) with videos related to

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Pageof 2

American Heart Journal|February 1, 1997

Hereditary bundle branch defect: right bundle branch blocks of different causes have different morphologic characteristicsE Stéphan, A de Meeus, P Bouvagnet

Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992

A detailed linkage map of subtelomeric murine chromosome 12 region including the situs inversus mutation locus IVA de Meeus, S Alonso, J Demaille, et al.

Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1993

[Mice SI/Col: a study model in the research of genes involved in situs inversus]A de Meeus, S Alonso, J Demaille, et al.

Acta Neurologica Belgica|September 1, 1978

[Ventriculo-cardiac derivation in late complications of hemispherectomy (author's transl)]J Achslogh, J P Boucquey, A de Meeus, et al.

Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1996

[Genetics of hereditary cardiopathies]S Debrus, A de Meeus, M K Jean, et al.

American Journal of Medical Genetics|February 11, 1997

Blastogenesis dominant 1: a sequence with midline anomalies and heterotaxyA de Meeus, P Sarda, R Tenconi, et al.

Neuroradiology|August 25, 1977

The management of anterior sacral meningocele with computed tomographyD Balériaux-Waha, M Osteaux, G Terwinghe, et al.

Journal of Medical Genetics|July 25, 1998

Linkage disequilibrium between the M470V variant and the IVS8 polyT alleles of the CFTR gene in CBAVDA de Meeus, C Guittard, M Desgeorges, et al.

Human Mutation|April 13, 1999

Genetic findings in congenital bilateral aplasia of vas deferens patients and identification of six novel mutatations. Mutations in brief no. 138. OnlineA de Meeus, C Guittard, M Desgeorges, et al.

Journal Francais D'Ophtalmologie|October 6, 1998

[Clinical features and genetic analysis in a family with X-linked incomplete congenital stationary night blindness (CSNBi)]C F Schmitt-Bernard, C Bareil, C P Hamel, et al.

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