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Molecular and Cellular Probes|August 31, 2014
Point mutation frequency in the FMR1 gene as revealed by fragile X syndrome screeningMaximilian Handt, Andrea Epplen, Sabine Hoffjan, et al.Molecular Vision|March 1, 2007
Haplotype-defined linkage region for gPRA in Schapendoes dogsTanja Lippmann, Anna Jonkisz, Tadeusz Dobosz, et al.Molecular Syndromology|May 20, 2016
A Novel ECM1 Splice Site Mutation in Lipoid Proteinosis: Case Report plus Review of the LiteratureLinda K Rey, Jürgen Kohlhase, Katrin Möllenhoff, et al.BMC Neurology|January 11, 2018
Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypesGülsah Aydin, Gabriele Dekomien, Sabine Hoffjan, et al.Pain|June 24, 2006
Muscle pain in myophosphorylase deficiency (McArdle's disease): the role of gender, genotype, and pain-related copingOliver Rommel, Rudolf A Kley, Gabriele Dekomien, et al.Molecular and Cellular Probes|November 15, 2013
High creatine kinase levels and white matter changes: clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiencyMaria de los Angeles Beytía, Gabriele Dekomien, Sabine Hoffjan, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 16, 2014
LAMA2-related congenital muscular dystrophy complicated by West syndromeAna Camacho, Noemí Núñez, Gabriele Dekomien, et al.Journal of Geriatric Psychiatry and Neurology|March 27, 2009
APOE alleles in Parkinson disease and their relationship to cognitive decline: a population-based, longitudinal studyMartin Wilhelm Kurz, Gabriele Dekomien, Odd Bjarte Nilsen, et al.Neuromuscular Disorders : NMD|January 27, 2009
Eosinophilic myositis as presenting symptom in gamma-sarcoglycanopathySarah K Baumeister, Slobodanka Todorovic, Vedrana Milić-Rasić, et al.Journal of the Neurological Sciences|January 17, 2015
Analysis of the C19orf12 and WDR45 genes in patients with neurodegeneration with brain iron accumulationAnne Tschentscher, Gabriele Dekomien, Sophia Ross, et al.Pageof 5