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Exome sequencing in four families with neurodevelopmental disorders: genotype-phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN.
Afridi TUK, Fatima A, Satti HS, Akram Z, Yousafzai IK, Naeem WB, Fatima N, Ali A, Iqbal Z, Khan A, Shahzad M, Liu C, Toft M, Zhang F, Tariq M, Davis EE, Khan TN. Afridi TUK, et al. Among authors: ali a. Mol Genet Genomics. 2024 May 21;299(1):55. doi: 10.1007/s00438-024-02149-y. Mol Genet Genomics. 2024. PMID: 38771357
Multi-institutional Protocol Guidance for Pediatric Photon-counting CT.
Horst KK, Cao JY, McCollough CH, El-Ali A, Frush DP, Siegel MJ, Ramirez-Giraldo JC, O'Donnell T, Bach S, Yu L. Horst KK, et al. Among authors: el ali a. Radiology. 2024 May;311(2):e231741. doi: 10.1148/radiol.231741. Radiology. 2024. PMID: 38771176 Review.
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