A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation von Abu-Amero, Khaled K, Hellani, Ali M, Salih, Mustafa A, Seidahmed, Mohammad Z, Elmalik, Tageldin S, Zidan, Ghassan, Bosley, Thomas M

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Clinical and molecular characterization of maturity onset-diabetes of the young caused by hepatocyte nuclear factor-4 alpha mutation: red flags for prediction of the diagnosis von Mohamed, Sarar, Elkholy, Susan, El-Meleagy, Ebtessam, Abu-Amero, Khaled, Hellani, Ali M

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Neurologic Injury in Isolated Sulfite Oxidase Deficiency von Bosley, Thomas M., Alorainy, Ibrahim A., Oystreck, Darren T., Hellani, Ali M., Seidahmed, Mohammed Z., Osman, Mohamed El Faki, Sabry, Mohamed A., Rashed, Mohamed S., Al-Yamani, Eiman A., Abu-Amero, Khaled K., Salih, Mustafa A.

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High-resolution analysis of DNA copy number alterations in patients with isolated sporadic keratoconus von Abu-Amero, Khaled K, Hellani, Ali M, Al Mansouri, Sameer M, Kalantan, Hatem, Al-Muammar, Abdulrahman M

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Preimplantation Genetic Diagnosis in Isolated Sulfite Oxidase Deficiency von Salih, Mustafa A., Bosley, Thomas M., Alorainy, Ibrahim A., Sabry, Mohamed A., Rashed, Mohamed S., Al-Yamani, Eiman A., El-Akoum, Siham, Mohamed, Sarar H., Abu-Amero, Khaled K., Hellani, Ali M.

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Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder von Abu-Amero, Khaled K, Kondkar, Altaf A, Hellani, Ali M, Bosley, Thomas M, Khan, Arif O

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Successful pregnancies after combined human leukocyte antigen direct genotyping and preimplantation genetic diagnosis utilizing multiple displacement amplification von HELLANI, Ali M, AKOUM, Siham M, FADEL, Elias S, YOUSEF, Hisham M, ABU-AMERO, Khaled K

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A new era for preventive genetic programs in the Arabian Peninsula von AL-ODAIB, Ali N, ABU-AMERO, Khaled K, OZAND, Pinar T, AL-HELLANI, Ali M

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Hemoglobin D/β-thalassemia and β-thalassemia major in a Saudi family von OWAIDAH, Tarek M, AL-SALEH, Mahasen M, AL-HELLANI, Ali M

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Recently Available Techniques Applicable to Genetic Problems in the Middle East von Ozand, Pinar T., Odaib, Ali Al, Sakati, Nadia, Al-Hellani, Ali M.

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Lateral dislocation of the elbow joint in children: a case report von Missaoui, Zied, Moussa, Mohamad K., Pouzenc, Lucas, Hellani, Ali A., Alayane, Ali

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Minimally invasive percutaneous plate osteosynthesis for treatment of proximal humeral shaft fractures von Chamseddine, Ali Hassan, El-Hajj, Oussama M., Haidar, Ibrahim M., Rahal, Mohammad Jawad H., Farhat, Hussein S., Hellani, Ali A., Asfour, Ali H., Zeyneddin, Mariam M.

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Androgens and Postmeiotic Germ Cells Regulate Claudin-11 Expression in Rat Sertoli Cells von Florin, Anne, Maire, Magali, Bozec, Aline, Hellani, Ali, Chater, Sonia, Bars, Remi, Chuzel, Franck, Benahmed, Mohamed

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Multiple displacement amplification on single cell and possible PGD applications von Hellani, Ali, Coskun, Serdar, Benkhalifa, Moncef, Tbakhi, Abelghani, Sakati, Nadia, Al-Odaib, Ali, Ozand, Pinar

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Down-regulation of OPA1 in patients with primary open angle glaucoma von Bosley, Thomas M, Hellani, Ali, Spaeth, George L, Myers, Jonathan, Katz, L Jay, Moster, Marlene R, Milcarek, Barry, Abu-Amero, Khaled K

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Genome-wide expression profile of LHON patients with the 11778 mutation von Abu-Amero, Khaled K, Jaber, Mohammad, Hellani, Ali, Bosley, Thomas M

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Five new consanguineous families with horizontal gaze palsy and progressive scoliosis and novel ROBO3 mutations von Abu-Amero, Khaled K, Dhalaan, Hesham al, Zayed, Zayed al, Hellani, Ali, Bosley, Thomas M

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Choroid plexus papilloma metastases to both cerebellopontine angles mimicking neurofibromatosis type 2 von Al-Abdullah, Abdulelah A., Abu-Amero, Khaled K., Hellani, Ali, Alkhalidi, Hisham, Bosley, Thomas M.

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A t(5; 16)(p15.32; q23.3) generating 16q23.3 RT qter duplication and 5p15.32 RT pter deletion in two siblings with mental retardation, dysmorphic features, and speech delay von Hellani, Ali, Mohamed, Sarar, Al-Akoum, Siham, Bosley, Thomas M, Abu-Amero, Khaled K

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At(5;16) (p15.32;q23.3) Generating 16q23.3 → qter Duplication and 5p15.32 → pter Deletion in Two Siblings With Mental Retardation, Dysmorphic Features, and Speech Delay von HELLANI, Ali, MOHAMED, Sarar, AL-AKOUM, Siham, BOSLEY, Thomas M, ABU-AMERO, Khaled K

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