L Bachner - JoVE Visualize

Showing results (11-20 of 24) with videos related to

Pageof 3

Sort By:

Human Genetics|July 1, 1990

Linkage study of a large family with autosomal dominant polycystic kidney disease with reduced expression. Absence of linkage to the PKD 1 locusL Bachner, M C Vinet, R Lacave, et al.

Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|November 1, 1993

Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysisC Dodé, A Dürr, C Pêcheux, et al.

Journal of Medical Genetics|April 1, 1994

Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north AfricaF el Kerch, A Sefiani, K Azibi, et al.

Nature Genetics|July 1, 1994

Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cenK Zerres, G Mücher, L Bachner, et al.

Human Molecular Genetics|September 1, 1993

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12K Azibi, L Bachner, J S Beckmann, et al.

American Journal of Human Genetics|November 1, 1995

Mapping of a gene for long QT syndrome to chromosome 4q25-27J J Schott, F Charpentier, S Peltier, et al.

Genomics|May 1, 1992

Fine genetic localization of the gene for autosomal dominant polycystic kidney disease (PKD1) with respect to physically mapped markersS Somlo, B Wirth, G G Germino, et al.

American Journal of Human Genetics|April 1, 1997

A gene for dominant nonspecific X-linked mental retardation is located in Xq28V des Portes, P Billuart, A Carrié, et al.

American Journal of Human Genetics|May 23, 1998

Mapping of a congenital microcoria locus to 13q31-q32C Rouillac, O Roche, D Marchant, et al.

Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1994

Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiencyN B Romero, F M Tomé, F Leturcq, et al.

Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:

Pageof 3

Human Genetics|July 1, 1990

Linkage study of a large family with autosomal dominant polycystic kidney disease with reduced expression. Absence of linkage to the PKD 1 locusL Bachner, M C Vinet, R Lacave, et al.

Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|November 1, 1993

Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysisC Dodé, A Dürr, C Pêcheux, et al.

Journal of Medical Genetics|April 1, 1994

Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north AfricaF el Kerch, A Sefiani, K Azibi, et al.

Nature Genetics|July 1, 1994

Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cenK Zerres, G Mücher, L Bachner, et al.

Human Molecular Genetics|September 1, 1993

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12K Azibi, L Bachner, J S Beckmann, et al.

American Journal of Human Genetics|November 1, 1995

Mapping of a gene for long QT syndrome to chromosome 4q25-27J J Schott, F Charpentier, S Peltier, et al.

Genomics|May 1, 1992

Fine genetic localization of the gene for autosomal dominant polycystic kidney disease (PKD1) with respect to physically mapped markersS Somlo, B Wirth, G G Germino, et al.

American Journal of Human Genetics|April 1, 1997

A gene for dominant nonspecific X-linked mental retardation is located in Xq28V des Portes, P Billuart, A Carrié, et al.

American Journal of Human Genetics|May 23, 1998

Mapping of a congenital microcoria locus to 13q31-q32C Rouillac, O Roche, D Marchant, et al.

Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 1, 1994

Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiencyN B Romero, F M Tomé, F Leturcq, et al.

Pageof 3