Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients von Mabrouk, Imed, Al-Harthi, Nawal, Mani, Rahma, Montantin, Guy, Tissier, Sylvie, Lagha, Rihab, Ben Abdallah, Fethi, Hassan, Mohamad M, Alhomrani, Majid, Gaber, Ahmed, Alsanie, Walaa F, Ouali, Hanadi, Jambi, Fatma A, Almaghamsi, Talal M, Alqarni, Nawal A, Alfarsi, Nawaf A, Kashgari, Khadija, Al-Zahrani, Hasna J, Al-Shamary, Zamel A, Al-Harbi, Abdullah, Amselem, Serge, Escudier, Estelle, Legendre, Marie

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Whole exome sequencing detects novel variants in Saudi children diagnosed with eczema von Bogari, Neda M., Amin, Amr A., Rayes, Husni H., Abdelmotelb, Ahmed, Al-Allaf, Faisal A., Dannoun, Anas, Al-Amodi, Hiba S., Sedayo, Anas A., Almalk, Hilal, Moulana, Amna, Balkhair, Rania, Jambi, Fatma, Madani, Fakhriah, Abutalib, Mwafaq, Taher, Mohiuddin M., Bouazzaoui, Abdellatif, Aljohani, Ashwag, Bogari, Mustafa N., G.K., Udaya Raja, Fawzy, Ahmed, Alharbi, Khalid Khalaf, Ali Khan, Imran

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