机译:细胞遗传学平衡染色体易位的全基因组测序识别出潜在的病理基因破坏,并突出了微观学学在地层机制中的重要性
Karolinska Inst Dept Mol Med &
Surg S-17176 Stockholm Sweden;
Karolinska Inst Dept Mol Med &
Surg S-17176 Stockholm Sweden;
Karolinska Inst Dept Mol Med &
Surg S-17176 Stockholm Sweden;
Karolinska Inst Dept Mol Med &
Surg S-17176 Stockholm Sweden;
Karolinska Inst Dept Mol Med &
Surg S-17176 Stockholm Sweden;
Karolinska Inst Dept Mol Med &
Surg S-17176 Stockholm Sweden;
Karolinska Inst Dept Mol Med &
Surg S-17176 Stockholm Sweden;
Karolinska Inst Dept Mol Med &
Surg S-17176 Stockholm Sweden;
Karolinska Inst Dept Mol Med &
Surg S-17176 Stockholm Sweden;
Karolinska Inst Dept Mol Med &
Surg S-17176 Stockholm Sweden;
KTH Royal Inst Technol Sch Biotechnol SciLifeLab S-17171 Stockholm Sweden;
KTH Royal Inst Technol Sch Biotechnol SciLifeLab S-17171 Stockholm Sweden;
Stockholm Univ Dept Biochem &
Biophys SciLifeLab S-17121 Stockholm Sweden;
Baylor Coll Med Dept Mol &
Human Genet Houston TX 77030 USA;
Karolinska Inst Dept Mol Med &
Surg S-17176 Stockholm Sweden;
Karolinska Inst Dept Mol Med &
Surg S-17176 Stockholm Sweden;
Baylor Coll Med Dept Mol &
Human Genet Houston TX 77030 USA;
Karolinska Inst Dept Mol Med &
Surg S-17176 Stockholm Sweden;
balanced chromosomal aberration; reciprocal translocation; whole-genome sequencing; microhomology; nonhomologous end joining; replication-based repair mechanisms;
机译:细胞遗传学平衡染色体易位的全基因组测序识别出潜在的病理基因破坏,并突出了微观学学在地层机制中的重要性
机译:通过浅全基因组测序点到EFNA5,BAHD1和PPP2R5E作为引起人类孟德利亚疾病的基因的新候选人
机译:全基因组低覆盖下一代测序检测和表征平衡染色体易位的临床应用
机译:核心材料中的生成水别测定的创新方法识别形成异质性和潜在损伤机制
机译:利用涉及A和D基因组某些染色体的杂合易位易位的突变,细胞组学研究了Histurium hirusutum和Gossypium barbardense chromosomes之间的分化。
机译:细胞遗传平衡染色体易位的全基因组测序可识别潜在的病理基因破坏并突出了微同源性在形成机制中的重要性
机译:通过浅全基因组测序点对eFNA5,BAHD1和PPP2R5E作为引起人类孟德尔疾病的基因的新候选人的浅层染色体旋转点映射