burgrave

n.

贵族；

Johann Gottfried Roesner
Rau von Holzhausen
Primary adhalinopathy (α‐sarcoglycanopathy) Clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive ...
Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by ...
Dincer, P. et al. A biochemical, genetic and clinical survey of autosomal recessive limb girdle muscular dystrophy in Turkey. Ann. N...
A biochemical, getetic and clinical survey of autosomal recessive limb girdle musculsr dystrophy in Turkey
Miyoshi-like distal myopathy with mutations in anoctamin 5 gene
Custom oligonucleotide array-based CGH: a reliable diagnostic tool for detection of exonic copy-number changes in multiple targeted ...
Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy
A point mutation in the glycerol kinase gene associated with a deletion in the dystrophin gene in a familial X-linked muscular dystr...