Xiao, B., Wang, L., Liu, H., Fan, Y., Xu, Y., Sun, Y., & Qiu, W. (2019). Uniparental isodisomy caused autosomal recessive diseases: NGS‐based analysis allows the concurrent detection of homogenous variants and copy‐neutral loss of heterozygosity. Mol Genet Genomic Med.
Citación estilo ChicagoXiao, Bing, Lili Wang, Huili Liu, Yanjie Fan, Yan Xu, Yu Sun, y Wenjuan Qiu. "Uniparental Isodisomy Caused Autosomal Recessive Diseases: NGS‐based Analysis Allows the Concurrent Detection of Homogenous Variants and Copy‐neutral Loss of Heterozygosity." Mol Genet Genomic Med 2019.
Cita MLAXiao, Bing, et al. "Uniparental Isodisomy Caused Autosomal Recessive Diseases: NGS‐based Analysis Allows the Concurrent Detection of Homogenous Variants and Copy‐neutral Loss of Heterozygosity." Mol Genet Genomic Med 2019.