I-2. FSHD clinical manifestations and molecular genetics: an update

समान संसाधन

• O-1. High frequency of hypomethylation in patients with fshd-like phenotype
  द्वारा: Sacconi, S, और अन्य
  प्रकाशित: (2009)
• I-1. Diagnosis and long-term treatment of “untreatable” neuromuscular patients, an update
  द्वारा: Engel, WK
  प्रकाशित: (2009)
• I-11. Genetic and environmental factors in amyotrophic lateral sclerosis
  द्वारा: Middleton, LT
  प्रकाशित: (2009)
• P-8. Molecular genetic studies of Charcot-Marie-Tooth disease in the Cypriot population
  द्वारा: Nicolaou, P, और अन्य
  प्रकाशित: (2009)
• P-1. Juvenile myasthenia gravis: genetic aspects
  द्वारा: Corsi, I, और अन्य
  प्रकाशित: (2009)