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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 26, 2012
Survival in Duchenne muscular dystrophySusanne Rall, Tiemo GrimmActa Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 27, 2013
Risk assessment and genetic counseling in families with Duchenne muscular dystrophyTiemo Grimm, Wolfram Kress, Gerhard Meng, et al.Neuromuscular Disorders : NMD|December 24, 2025
Becker muscular dystrophy (BMD) is caused by a dystrophin missense mutation in the original family of Becker and KienerWolfram Kress, Ute Hehr, Berthold Schalke, et al.American Journal of Human Genetics|April 16, 2002
Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier geneRalf Giess, Bettina Holtmann, Massimiliano Braga, et al.American Journal of Medical Genetics. Part A|March 19, 2008
Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophyBirgit Zirn, Wolfram Kress, Tiemo Grimm, et al.Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|August 21, 2020
[Genetic counseling in Germany: development of demand]Jörg Schmidtke, Jörg T Epplen, Ralf Glaubitz, et al.American Journal of Human Genetics|December 9, 2008
PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruptionEva Decker, Angelika Stellzig-Eisenhauer, Britta S Fiebig, et al.L' Orthodontie Francaise|September 3, 2013
[Primary failure of eruption (PFE). Clinical and molecular genetics analysis]Angelika Stellzig-Eisenhauer, Eva Decker, Philipp Meyer-Marcotty, et al.Journal of Orofacial Orthopedics = Fortschritte Der Kieferorthopadie : Organ/Official Journal Deutsche Gesellschaft Fur Kieferorthopadie|February 6, 2010
Primary failure of eruption (PFE)--clinical and molecular genetics analysisAngelika Stellzig-Eisenhauer, Eva Decker, Philipp Meyer-Marcotty, et al.International Journal of Cancer|April 5, 2014
Validation of the Manchester scoring system for predicting BRCA1/2 mutations in 9,390 families suspected of having hereditary breast and ovarian cancerKarin Kast, Rita K Schmutzler, Kerstin Rhiem, et al.Pageof 2