Reanalysis of exome sequencing data of intellectual disability samples: Yields and benefits von Al‐Nabhani, Maryam, Al‐Rashdi, Samiya, Al‐Murshedi, Fathiya, Al‐Kindi, Adila, Al‐Thihli, Khalid, Al‐Saegh, Abeer, Al‐Futaisi, Amna, Al‐Mamari, Watfa, Zadjali, Fahad, Al‐Maawali, Almundher

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Further phenotypic delineation of Alazami syndrome von Al‐Hinai, Abdulhamid, Al‐Hashmi, Samiya, Ganesh, Anuradha, Al‐Hashmi, Nadia, Al‐Saegh, Abeer, Al‐Mamari, Watfa, Al‐Murshedi, Fathiya, Al‐Thihli, Khalid, Al‐Kindi, Adila, Al‐Maawali, Almundher

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Variability of non‐lethal Fowler syndrome phenotype associated with FLVCR2 variants von Al‐Murshedi, Fathiya, Mirza, Hassan, Al‐Saegh, Abeer, Al‐Nabhani, Maryam, Al‐Shabibi, Saud, Baawain, Saleh, Al‐Futaisi, Amna, Al‐Shehhi, Wafaa, Al‐Maawali, Almundher

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Strengthening evidence to inform health systems: opportunities for the WHO and partners to accelerate progress on non-communicable diseases von Hyder, Adnan A, Rylance, Sarah, Al Saegh, Abeer, Feigin, Valery L, Kataria, Ishu, Laatikainen, Tiina, Lee, Liming, Mahendradhata, Yodi, Marten, Robert, Mikkelsen, Bente, Miranda, J Jaime, Nugent, Rachel, Owolabi, Mayowa, Sullivan, Richard, Virani, Salim S, Reddy, K Srinath, Saegh, Abeer Al, Feigin, Valery, Hyder, Adnan A, Laatikainen, Tiina, Li, Liming, Mahendradhata, Yodi, Jaime Miranda, J, Owolabi, Mayowa, Reddy, Srinath, Sullivan, Richard, Virani, Salim S

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Biallelic PTRHD1 Frameshift Variants Associated with Intellectual Disability, Spasticity, and Parkinsonism von Al‐Kasbi, Ghalia, Al‐Saegh, Abeer, Al‐Qassabi, Ahmed, Al‐Jabry, Tariq, Zadjali, Fahad, Al‐Yahyaee, Said, Al‐Maawali, Almundher

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The Manchester Scoring System for predicting BRCA1/2 mutations underperforms in Arabic Omani breast cancer patients von van Wyk, Chantel, Al-Sayegh, Hasan, Al-Kiyumi, Sara I, Al-Mamari, Ghaida S, Al Saegh, Abeer A

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The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families von Al-Kasbi, Ghalia, Al-Murshedi, Fathiya, Al-Kindi, Adila, Al-Hashimi, Nadia, Al-Thihli, Khalid, Al-Saegh, Abeer, Al-Futaisi, Amna, Al-Mamari, Watfa, Al-Asmi, Abdullah, Bruwer, Zandre, Al-Kharusi, Khalsa, Al-Rashdi, Samiya, Zadjali, Fahad, Al-Yahyaee, Said, Al-Maawali, Almundher

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Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family von Al-Amri, Ahmed, Saegh, Abeer Al, Al-Mamari, Watfa, El-Asrag, Mohammed E., Ivorra, Jose L., Cardno, Alastair G., Inglehearn, Chris F., Clapcote, Steven J., Ali, Manir

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Clinical and Molecular Characteristics of Children with Beckwith-Wiedemann Syndrome and Isolated Hemi Hyperplasia at Sultan Qaboos University Hospital with Their Surveillance Outco... von Al-Hinai, Ayat Sulayiam, Al-Maawali, Almundher, Al-Kindi, Adila, Al-Saegh, Abeer, Al-Thihli, Khalid, Otaify, Ghada A.

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Variability of non-lethal Fowler syndrome phenotype associated withFLVCR2variants von Al-Murshedi, Fathiya, Mirza, Hassan, Al-Saegh, Abeer, Al-Nabhani, Maryam, Al-Shabibi, Saud, Baawain, Saleh, Al-Futaisi, Amna, Al-Shehhi, Wafaa, Al-Maawali, Almundher

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Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of Patients with Autism Spectrum Disorders from a Highly Consanguineous Population von Al-Mamari, Watfa, Al-Saegh, Abeer, Al-Kindy, Adila, Bruwer, Zandre, Al-Murshedi, Fathiya, Al-Thihli, Khalid

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LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss von Al-Amri, Ahmed H., Al Saegh, Abeer, Al-Mamari, Watfa, El-Asrag, Mohammed E., Al-Kindi, Mohammed N., Al Khabouri, Mazin, Al Wardy, Nadia, Al Lamki, Khalsa, Gabr, Ahlam, Idris, Ahmed, Inglehearn, Chris F., Clapcote, Steven J., Ali, Manir

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Further phenotypic delineation of Alazami syndrome von Al-Hinai, Abdulhamid, Al-Hashmi, Samiya, Ganesh, Anuradha, Al-Hashmi, Nadia, Al-Saegh, Abeer, Al-Mamari, Watfa, Al-Murshedi, Fathiya, Al-Thihli, Khalid, Al-Kindi, Adila, Al-Maawali, Almundher

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