Diagnostic implications of pitfalls in causal variant identification based on 4577 molecularly characterized families von AlAbdi, L, Maddirevula, S, Shamseldin, HE, Khouj, E, Helaby, R, Hamid, H, Almulhim, A, Hashem, MO, Abdulwahab, F, Abouyousef, O, Alqahtani, M, Altuwaijri, N, Jaafar, A, Alshidi, T, Alzahrani, F, Al-Sagheir, AI, Mansour, AM, Alawaji, A, Aldhilan, A, Alhashem, A, Alhemidan, A, Nabil, A, Khan, AO, Aljohar, A, Alsaleem, B, Tabarki, B, Lourenco, CM, Faqeih, E, AlShail, E, Almesaifri, F, Mutairi, FA, Alzaidan, H, Morsy, H, Alshihry, H, Alkuraya, H, Girisha, KM, Al-Fayez, K, Al-Rubeaan, K, kraoua, L, Alnemer, M, Tulbah, M, Zaki, MS, Alfadhel, M, Abouelhoda, M, Nezarati, MM, Al-Qattan, M, Shboul, M, Abanemai, M, Al-Muhaizea, MA, Al-owain, M, Bafaqeeh, MS, Alshammari, M, Abukhalid, M, Alsahan, N, Derar, N, Meriki, N, Bohlega, SA, Tala, SA, Alhassan, S, Wali, S, Mohamed, S, Coskun, S, Saadeh, S, Tkemaladze, T, Kurdi, W, Alhumaidi, ZA, Rahbeeni, Z, Alkuraya, FS

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Diagnostic implications of pitfalls in causal variant identification based on 4577 molecularly characterized families von AlAbdi, Lama, Maddirevula, Sateesh, Shamseldin, Hanan E., Khouj, Ebtissal, Helaby, Rana, Hamid, Halima, Almulhim, Aisha, Hashem, Mais O., Abdulwahab, Firdous, Abouyousef, Omar, Alqahtani, Mashael, Altuwaijri, Norah, Jaafar, Amal, Alshidi, Tarfa, Alzahrani, Fatema, Alkuraya, Fowzan S.

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Beyond the exome: utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases von AlAbdi, Lama, Shamseldin, Hanan E, Khouj, Ebtissal, Helaby, Rana, Aljamal, Bayan, Alqahtani, Mashael, Almulhim, Aisha, Hamid, Halima, Hashem, Mais O, Abdulwahab, Firdous, Abouyousef, Omar, Jaafar, Amal, Alshidi, Tarfa, Al-Owain, Mohammed, Alhashem, Amal, Al Tala, Saeed, Khan, Arif O, Mardawi, Elham, Alkuraya, Hisham, Faqeih, Eissa, Afqi, Manal, Alkhalifi, Salwa, Rahbeeni, Zuhair, Hagos, Samya T, Al-Ahmadi, Wijdan, Nadeef, Seba, Maddirevula, Sateesh, Khabar, Khalid S A, Putra, Alexander, Angelov, Angel, Park, Changsook, Reyes-Ramos, Ana M, Umer, Husen, Ullah, Ikram, Driguez, Patrick, Fukasawa, Yoshinori, Cheung, Ming Sin, Gallouzi, Imed Eddine, Alkuraya, Fowzan S

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Arab founder variants: Contributions to clinical genomics and precision medicine von AlAbdi, Lama, Maddirevula, Sateesh, Aljamal, Bayan, Hamid, Halima, Almulhim, Aisha, Hashem, Mais O., Algoos, Yusra, Alqahtani, Mashael, Albaloshi, Shahad, Alghamdi, Mohammed, Alduaylij, Mohammed, Shamseldin, Hanan E., Nadeef, Seba, Patel, Nisha, Abdulwahab, Firdous, Abouyousef, Omar, Alshidi, Tarfa, Jaafar, Amal, Abouelhoda, Mohamed, Alhazzani, Adel, Alfares, Ahmed, Qudair, Ahmad, Alsulaiman, Ahood, Alhashem, Amal, Khan, Arif O., Chedrawi, Aziza, Alebdi, Basel, AlAjlan, Fahad, Alotaibi, Fawaz, Alzaidan, Hamad, Banjar, Hanaa, Abdelraouf, Hanem, Alkuraya, Hisham, Abumansour, Iman, Alfayez, Khowlah, Tulbah, Maha, Alowain, Mohammed, Alqahtani, Mohammed, El-Kalioby, Mohammed, Shboul, Mohammad, Sulaiman, Raashda, Al Tala, Saed, Khan, Sameena, Coskun, Serdar, Mrouge, Sobaihi, Alenazi, Walaa, Rahbeeni, Zuhair, Alkuraya, Fowzan S.

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