The experience of Preimplantation Genetic Testing (PGT) among Muslim couples in Oman in the Middle East von Al‐Kharusi, Khalsa, Bruwer, Zandre, Wessels, Tina‐Marié

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Deficiency of acyl‐CoA synthetase 5 is associated with a severe and treatable failure to thrive of neonatal onset von Al‐Thihli, Khalid, Afting, Cassian, Al‐Hashmi, Nadia, Mohammed, Mohammed, Sliwinski, Svenja, Al Shibli, Naema, Al‐Said, Khoula, Al‐Kasbi, Ghalia, Al‐Kharusi, Khalsa, Merle, Uta, Füllekrug, Joachim, Al‐Maawali, Almundher

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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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Occurrence of Optic Neuritis and Cervical Cord Schwannoma with Charcot-Marie-Tooth Type 4B1 Disease von Al-Murshedi , Fathiya, Bruwer , Zandre, Al-Kharusi , Khalsa, Meftah , Douja, Scott , Patrick

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Uptake of prenatal genetic diagnosis and termination of pregnancy by Omani Muslim families at risk of genetic disorders: experience over a 9-year period von Bruwer, Zandré, Al Ubaidani, Salwa, Al Kharusi, Khalsa, Al Murshedi, Fathiya, Al-Maawali, Almundher, Al Sayegh, Abeer, Al Kindy, Adila, Al Riyami, Nihal, Al Dughaishi, Tamima, Al Salmani, Mouza, Al Hashmi, Nadia, Al Shehhi, Maryam, Al Fahdi, Badriya, Al Amri, Sumaya, Al-Thihli, Khalid

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Genetic counseling development and milestone in Oman von Al-Kharusi, Khalsa, Van Wyk, Chantel, Al Hinai, Mariya, Al-Fori, Amel, Bruwer, Zandre

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Biallelic loss-of-function variants of GFRA1 cause lethal bilateral renal agenesis von Al-Shamsi, Bushra, Al-Kasbi, Ghalia, Al-Kindi, Adila, Bruwer, Zandre, Al-Kharusi, Khalsa, Al-Maawali, Almundher

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IDENTIFICATION OF PROGNOSIS MARKERS IN PEDIATRIC HIGH-RISK ACUTE LYMPHOBLASTIC LEUKEMIA von Al-Lamki, Zakia, Wali, Yasser A., Wasifuddin, Shah M., Zachariah, Mathew, Al-Mjeni, Rayhanah, Li, Changping, Muralitharan, Shanmugakonar, Al-Kharusi, Khalsa, Gunaratne, Preethi, Peterson, Leif, Gibbs, Richard, Gingras, Marie-Claude, Margolin, Judith F.

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Trinucleotide repeat analysis of spinocerebellar ataxia patients in Oman von Chacko, Jacob P, Muralitharan, Shanmugakonar, Al-Ansari, Alia, Al-Kharusi, Khalsa, Al-Asmi, Abdullah, Pratap, Chand R, Bayoumi, Riad

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Occurrence of Optic Neuritis and Cervical Cord Schwannoma with Charcot-Marie-Tooth Type 4B1 Disease von Scott, Patrick, Bruwer, Zandre, Al-Kharusi, Khalsa, Meftah, Douja, Al-Murshedi, Fathiya

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