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Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients.
Mabrouk I, Al-Harthi N, Mani R, Montantin G, Tissier S, Lagha R, Ben Abdallah F, Hassan MM, Alhomrani M, Gaber A, Alsanie WF, Ouali H, Jambi FA, Almaghamsi TM, Alqarni NA, Alfarsi NA, Kashgari K, Al-Zahrani HJ, Al-Shamary ZA, Al-Harbi A, Amselem S, Escudier E, Legendre M. Mabrouk I, et al. Among authors: alqarni na. 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
Complications After Surgical Repair of Congenital Heart Disease in Infants. An Experience From Tertiary Care Center.
Javed F, Aleysae NA, Al-Mahbosh AY, Zubani AA, Atash AM, Salem HB, Abdallah M, Alkhatib O, Abu-Adas A, Hrays MA, Alqarni NA, Felemban A, Alsaedi SA, Jamjoom AA. Javed F, et al. Among authors: alqarni na. J Saudi Heart Assoc. 2021 Oct 15;33(4):271-278. doi: 10.37616/2212-5043.1267. eCollection 2021. J Saudi Heart Assoc. 2021. PMID: 35083116 Free PMC article.