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Manfred S Wehnert

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Seminars in Pediatric Neurology|July 26, 2002
The nuclear muscular dystrophiesManfred S Wehnert, Giséle Bonne
Biochemical Society Transactions|November 23, 2011
The LINC complex and human diseasePeter Meinke, Thuy Duong Nguyen, Manfred S Wehnert
Saudi Medical Journal|January 14, 2009
Restrictive dermopathy. Molecular diagnosis of restrictive dermopathy in a stillborn fetus from a consanguineous Iranian familyAriana Kariminejad, Peyman Goodarzi, Le Thi Thanh Huong, et al.
Neuromuscular Disorders : NMD|January 11, 2005
Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophyMaggie C Walter, Thomas N Witt, Beate Schlotter Weigel, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Early onset of cardiomyopathy in two brothers with X-linked Emery-Dreifuss muscular dystrophyUlvi Astra Talkop, Inga Talvik, Margit Sõnajalg, et al.
Basic Research in Cardiology|September 17, 2008
Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathyAndreas Perrot, Shwan Hussein, Volker Ruppert, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Seminars in Pediatric Neurology|July 26, 2002
The nuclear muscular dystrophiesManfred S Wehnert, Giséle Bonne
Biochemical Society Transactions|November 23, 2011
The LINC complex and human diseasePeter Meinke, Thuy Duong Nguyen, Manfred S Wehnert
Saudi Medical Journal|January 14, 2009
Restrictive dermopathy. Molecular diagnosis of restrictive dermopathy in a stillborn fetus from a consanguineous Iranian familyAriana Kariminejad, Peyman Goodarzi, Le Thi Thanh Huong, et al.
Neuromuscular Disorders : NMD|January 11, 2005
Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophyMaggie C Walter, Thomas N Witt, Beate Schlotter Weigel, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Early onset of cardiomyopathy in two brothers with X-linked Emery-Dreifuss muscular dystrophyUlvi Astra Talkop, Inga Talvik, Margit Sõnajalg, et al.
Basic Research in Cardiology|September 17, 2008
Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathyAndreas Perrot, Shwan Hussein, Volker Ruppert, et al.
Pageof 1