Search Results - Jambi, Fatma

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    Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients

    Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients by 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

    Whole exome sequencing detects novel variants in Saudi children diagnosed with eczema by 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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