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M Wehnert

Showing results (41-50 of 45) with videos related to

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Human Molecular Genetics|August 1, 1995
Isolation of chromosome-specific genes by reciprocal probing of arrayed cDNA and cosmid librariesC C Lee, A Yazdani, M Wehnert, et al.
Human Molecular Genetics|May 23, 1998
Mutations in Emery-Dreifuss muscular dystrophy and their effects on emerin protein expressionS Manilal, D Recan, C A Sewry, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25J Meulemann, G Kuhlenbäumer, A Schirmacher, et al.
Muscle & Nerve|September 17, 2004
Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutationsA Muchir, J Medioni, M Laluc, et al.
Annals of Neurology|August 12, 2000
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C geneG Bonne, E Mercuri, A Muchir, et al.
Pageof 5

Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Human Molecular Genetics|August 1, 1995
Isolation of chromosome-specific genes by reciprocal probing of arrayed cDNA and cosmid librariesC C Lee, A Yazdani, M Wehnert, et al.
Human Molecular Genetics|May 23, 1998
Mutations in Emery-Dreifuss muscular dystrophy and their effects on emerin protein expressionS Manilal, D Recan, C A Sewry, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25J Meulemann, G Kuhlenbäumer, A Schirmacher, et al.
Muscle & Nerve|September 17, 2004
Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutationsA Muchir, J Medioni, M Laluc, et al.
Annals of Neurology|August 12, 2000
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C geneG Bonne, E Mercuri, A Muchir, et al.
Pageof 5