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Human Genomics|October 23, 2022
Biallelic mutations of TTC12 and TTC21B were identified in Chinese patients with multisystem ciliopathy syndromesWeicheng Chen, Feifei Wang, Weijia Zeng, et al.
Human Genomics|September 18, 2022
Novel clinical, molecular and bioinformatics insights into the genetic background of autismIoanna Talli, Nikolas Dovrolis, Anastasis Oulas, et al.
Human Genomics|September 2, 2022
Characterization of ACE2 naturally occurring missense variants: impact on subcellular localization and traffickingSally Badawi, Feda E Mohamed, Nesreen R Alkhofash, et al.
Human Genomics|February 6, 2022
Frequencies of CYP2D6 genetic polymorphisms in Arab populationsMousa Alali, Wouroud Ismail Al-Khalil, Sara Rijjal, et al.
Human Genomics|October 5, 2018
Impact of ZBTB7A hypomethylation and expression patterns on treatment response to hydroxyureaVasiliki Chondrou, Eleana F Stavrou, Georgios Markopoulos, et al.
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