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Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients.
J Hum Genet. 2022 Jul;67(7):381-386. doi: 10.1038/s10038-021-01006-9. Epub 2022 Jan 20.
J Hum Genet. 2022.
PMID: 35046476
Whole exome sequencing detects novel variants in Saudi children diagnosed with eczema.
Bogari NM, Amin AA, Rayes HH, Abdelmotelb A, Al-Allaf FA, Dannoun A, Al-Amodi HS, Sedayo AA, Almalk H, Moulana A, Balkhair R, Jambi F, Madani F, Abutalib M, Taher MM, Bouazzaoui A, Aljohani A, Bogari MN, G K UR, Fawzy A, Alharbi KK, Ali Khan I.
Bogari NM, et al. Among authors: jambi f.
J Infect Public Health. 2020 Jan;13(1):27-33. doi: 10.1016/j.jiph.2019.05.020. Epub 2019 Jun 15.
J Infect Public Health. 2020.
PMID: 31213409
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