权威例句
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricul...
Longitudinal MRI study of hippocampal volume in trauma survivors with PTSD.
Nuclear lamins: laminopathies and their role in premature ageing
Cardiac myosin binding protein|[ndash]|C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy
Transgenic maize plants by tissue electroporation.
“Laminopathies:” a wide spectrum of human diseases
Double heterozygosity for mutations in the β-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with ...
Three hundred ways to assess Europe's surface waters: An almost complete overview of biological methods to implement the Water Frame...