APA Alıntı

Qiao, F., Zhang, C., Wang, Y., Liu, G., Shao, B., Hu, P., & Xu, Z. (2021). Case Report: Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL in a Fetus With Cornelia de Lange Syndrome. Front Genet.

Chicago Stili Alıntı

Qiao, Fengchang, Cuiping Zhang, Yan Wang, Gang Liu, Binbin Shao, Ping Hu, ve Zhengfeng Xu. "Case Report: Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL in a Fetus With Cornelia De Lange Syndrome." Front Genet 2021.

MLA Alıntı

Qiao, Fengchang, et al. "Case Report: Prenatal Whole-Exome Sequencing to Identify a Novel Heterozygous Synonymous Variant in NIPBL in a Fetus With Cornelia De Lange Syndrome." Front Genet 2021.