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Acta Neurologica Scandinavica|May 7, 2005

Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysisJ Infante, O Combarros, V Volpini, et al.

Neuromuscular Disorders : NMD|November 11, 2008

Two Spanish families with Charcot-Marie-Tooth type 2A: clinical, electrophysiological and molecular findingsI Banchs, C Casasnovas, J Montero, et al.

Clinical Genetics|November 15, 2006

Clinical and molecular analysis of X-linked Charcot-Marie-Tooth disease type 1 in Spanish populationC Casasnovas, I Banchs, J Corral, et al.

Neuroscience Letters|December 31, 2002

Understanding the dynamics of Spinocerebellar Ataxia 8 (SCA8) locus through a comparative genetic approach in humans and apesA M Andrés, M Soldevila, N Saitou, et al.

Medicina Clinica|July 12, 2001

[Analysis of psoriasis susceptibility regions in the Spanish population: evidence of a major gene involved in psoriasis in the 6p21 region]R de Cid, V Volpini, L Almasy, et al.

Medicina Clinica|June 5, 1998

[Clinical, genetic and molecular studies on autosomal dominant polycystic kidney disease]R Torra, C Badenas, A Darnell, et al.

Prenatal Diagnosis|March 1, 1994

Prenatal diagnosis of Werdnig-Hoffmann disease: DNA analysis of a mummified umbilical cord using closely linked microsatellite markersT Matilla, J Corral, M Miranda, et al.

Journal of the American Society of Nephrology : JASN|October 1, 1996

Linkage, clinical features, and prognosis of autosomal dominant polycystic kidney disease types 1 and 2R Torra, C Badenas, A Darnell, et al.

Human Mutation|January 1, 1997

The repeat expansion detection method in the analysis of diseases with CAG/CTG repeat expansion: usefulness and limitationsL Martorell, M A Pujana, V Volpini, et al.

American Journal of Medical Genetics|February 15, 2001

Linkage analysis in Spanish families with nonspecific X-linked mental retardation: Significant linkage at Xq13-q21C Badenas, S Castellví-Bel, V Volpini, et al.

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Showing results (11-20 of 55) with videos related to

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Acta Neurologica Scandinavica|May 7, 2005

Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysisJ Infante, O Combarros, V Volpini, et al.

Neuromuscular Disorders : NMD|November 11, 2008

Two Spanish families with Charcot-Marie-Tooth type 2A: clinical, electrophysiological and molecular findingsI Banchs, C Casasnovas, J Montero, et al.

Clinical Genetics|November 15, 2006

Clinical and molecular analysis of X-linked Charcot-Marie-Tooth disease type 1 in Spanish populationC Casasnovas, I Banchs, J Corral, et al.

Neuroscience Letters|December 31, 2002

Understanding the dynamics of Spinocerebellar Ataxia 8 (SCA8) locus through a comparative genetic approach in humans and apesA M Andrés, M Soldevila, N Saitou, et al.

Medicina Clinica|July 12, 2001

[Analysis of psoriasis susceptibility regions in the Spanish population: evidence of a major gene involved in psoriasis in the 6p21 region]R de Cid, V Volpini, L Almasy, et al.

Medicina Clinica|June 5, 1998

[Clinical, genetic and molecular studies on autosomal dominant polycystic kidney disease]R Torra, C Badenas, A Darnell, et al.

Prenatal Diagnosis|March 1, 1994

Prenatal diagnosis of Werdnig-Hoffmann disease: DNA analysis of a mummified umbilical cord using closely linked microsatellite markersT Matilla, J Corral, M Miranda, et al.

Journal of the American Society of Nephrology : JASN|October 1, 1996

Linkage, clinical features, and prognosis of autosomal dominant polycystic kidney disease types 1 and 2R Torra, C Badenas, A Darnell, et al.

Human Mutation|January 1, 1997

The repeat expansion detection method in the analysis of diseases with CAG/CTG repeat expansion: usefulness and limitationsL Martorell, M A Pujana, V Volpini, et al.

American Journal of Medical Genetics|February 15, 2001

Linkage analysis in Spanish families with nonspecific X-linked mental retardation: Significant linkage at Xq13-q21C Badenas, S Castellví-Bel, V Volpini, et al.

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