Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
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.
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