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Journal of Child Neurology|December 17, 2013
A paucisymptomatic neuromuscular disease mimicking type III 5q-SMA with complex rearrangements in the SMN geneLaura Nanna Lohkamp, Katja von Au, Hans-Hilmar Goebel, et al.
Familial Cancer|July 22, 2006
Low frequency of CHEK2 mutations in familial pancreatic cancerDetlef K Bartsch, Kristina Krysewski, Mercedes Sina-Frey, et al.
Chest|September 16, 2018
Impact of Vasoactive Medications on ICU-Acquired Weakness in Mechanically Ventilated PatientsKrysta S Wolfe, Bhakti K Patel, Erica L MacKenzie, et al.
Environmental Microbiology|January 20, 2011
Is dinitrogen fixation significant in the Levantine Basin, East Mediterranean Sea?Tali Yogev, Eyal Rahav, Edo Bar-Zeev, et al.
Plos One|September 28, 2011
The roots of diversity: below ground species richness and rooting distributions in a tropical forest revealed by DNA barcodes and inverse modelingF Andrew Jones, David L Erickson, Moises A Bernal, et al.
British Journal of Haematology|July 1, 1997
Missense mutations at ALA-10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapyJ Oldenburg, E M Quenzel, U Harbrecht, et al.
Human Mutation|May 18, 2006
Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfoldingKatrin Wenzel, Miriam Carl, Andreas Perrot, et al.
Genomics|January 1, 1989
A genetic linkage map of five marker loci in and around the Duchenne muscular dystrophy locusJ D Chen, J F Hejtmancik, G Romeo, et al.
Biophysical Journal|September 12, 2025
Many dynein teams collectively generate high forces during the transport of large organellesSimon Wieland, Christina Steininger, David E Gitschier, et al.
Military Medicine|December 30, 2021
Prescription Patterns and Relationship to Pharmacogenomics Testing in the Military Health SystemDaniel J Selig, Jeffrey R Livezey, Geoffrey C Chin, et al.
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