Articles
Mitochondrial tRNA methylation in Alzheimer’s disease and progressive supranuclear palsy
The diagnostic yield of intellectual disability: combined whole genome low-coverage sequencing and medical exome sequencing
ERα-related chromothripsis enhances concordant gene transcription on chromosome 17q11.1-q24.1 in luminal breast cancer
Molecular diagnosis in recessive pediatric neurogenetic disease can help reduce disease recurrence in families
MyoMiner: explore gene co-expression in normal and pathological muscle
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