More importantly, 16 patients (5.3% of population) had a genomic profile likely to cause a Mendeliandisorder.
更重要的,16名患者(5.3%)有一个可以引起孟德尔疾病的基因组。
2
Based on the comprehensive embryonic genome, we effectively performed whole-genome Mendeliandisorder diagnosis and human leukocyte antigen matching tests.
基于综合的胚胎基因组,研究人员有效地进行了全基因组的孟德尔疾病诊断与人类白细胞抗原匹配试验。
3
Traditionally, the genetic diagnosis of a mendeliandisorder relied on the establishment of a clinical diagnosis followed by the sequencing of previously implicated genes.