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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Reply from the author von Seidahmed, Mohammad Z

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Rundataxin, a novel protein with RUN and diacylglycerol binding domains, is mutant in a new recessive ataxia von Assoum, Mirna, Salih, Mustafa A., Drouot, Nathalie, H'Mida-Ben Brahim, Dorra, Lagier-Tourenne, Clotilde, AlDrees, Abdulmajeed, Elmalik, Salah A., Ahmed, Taha S., Seidahmed, Mohammad Z., Kabiraj, Mohammad M., Koenig, Michel

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A case of fetal valproate syndrome with new features expanding the phenotype von Al-Mendalawi, Mahmood D, Seidahmed, Mohammad Z

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Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia von Tesson, Christelle, Nawara, Magdalena, Salih, Mustafa A.M., Rossignol, Rodrigue, Zaki, Maha S., Al Balwi, Mohammed, Schule, Rebecca, Mignot, Cyril, Obre, Emilie, Bouhouche, Ahmed, Santorelli, Filippo M., Durand, Christelle M., Oteyza, Andrés Caballero, El-Hachimi, Khalid H., Al Drees, Abdulmajeed, Bouslam, Naima, Lamari, Foudil, Elmalik, Salah A., Kabiraj, Mohammad M., Seidahmed, Mohammed Z., Esteves, Typhaine, Gaussen, Marion, Monin, Marie-Lorraine, Gyapay, Gabor, Lechner, Doris, Gonzalez, Michael, Depienne, Christel, Mochel, Fanny, Lavie, Julie, Schols, Ludger, Lacombe, Didier, Yahyaoui, Mohamed, Al Abdulkareem, Ibrahim, Zuchner, Stephan, Yamashita, Atsushi, Benomar, Ali, Goizet, Cyril, Durr, Alexandra, Gleeson, Joseph G., Darios, Frederic, Brice, Alexis, Stevanin, Giovanni

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The many faces of peroxisomal disorders: Lessons from a large Arab cohort von Alshenaifi, Jumanah, Ewida, Nour, Anazi, Shams, Shamseldin, Hanan E., Patel, Nisha, Maddirevula, Sateesh, Al‐Sheddi, Tarfa, Alomar, Rana, Alobeid, Eman, Ibrahim, Niema, Hashem, Mais, Abdulwahab, Firdous, Jacob, Minnie, Alhashem, Amal, Alzaidan, Hamad I., Seidahmed, Mohammed Z., Alhashemi, Nadia, Rawashdeh, Rifaat, Eyaid, Wafaa, Al‐Hassnan, Zuhair N., Rahbeeni, Zuhair, Alswaid, Abdulrahman, Hadid, Adnan, Qari, Alya, Mohammed, Dia A., El Khashab, Heba Y., Alfadhel, Majid, Abanemai, Mohammad, Sunbul, Rawda, Al Tala, Saeed, Alkhalifi, Salwa, Alkharfi, Turki, Abouelhoda, Mohamed, Monies, Dorota, Al Tassan, Nada, AlDubayan, Saud H., Kurdi, Wesam, Al‐Owain, Mohammed, Dasouki, Majed J., Kentab, Amal Y., Atyani, Suha, Makhseed, Nawal, Faqeih, Eissa, Shaheen, Ranad, Alkuraya, Fowzan S.

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Determination of urinary S-sulphocysteine, xanthine and hypoxanthine by liquid chromatography-electrospray tandem mass spectrometry von Rashed, Mohamed S., Saadallah, Amal A. A., Rahbeeni, Zuhair, Eyaid, Wafaa, Seidahmed, Mohamed Z., Al-Shahwan, Saad, Salih, Mustafa A. M., Osman, Mohammad E., Al-Amoudi, Mohamed, Al-Ahaidib, Lujane, Jacob, Minnie

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Determination of urinaryS-sulphocysteine, xanthine and hypoxanthine by liquid chromatography-electrospray tandem mass spectrometry von Rashed, Mohamed S., Saadallah, Amal A. A., Rahbeeni, Zuhair, Eyaid, Wafaa, Seidahmed, Mohamed Z., Al-Shahwan, Saad, Salih, Mustafa A. M., Osman, Mohammad E., Al-Amoudi, Mohamed, Al-Ahaidib, Lujane, Jacob, Minnie

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