Associated Papers
Saturation genome editing of RNU4-2 reveals distinct dominant and recessive neurodevelopmental disorders.
De Jonghe J et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
Whole-exome sequencing identifies FANC heterozygous germline mutation as an adverse factor for immunosuppressive therapy in Chinese aplastic anemia patients aged 40 or younger: a single-center retrospective study.
Shen Y et al.
Annals of Hematology, 2023
DNA excision repair and double-strand break repair gene polymorphisms and the level of chromosome aberration in children with long-term exposure to radon.
Larionov AV et al.
International Journal of Radiation Biology, 2016
Investigation of pathogenic genes in peri-implantitis from implant clustering failure patients: a whole-exome sequencing pilot study.
Lee S et al.
Plos One, 2014
24921256 (PubMed )
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