Novel homozygous mutation of PNLIP gene in congenital pancreatic lipase deficiency: an extended family study von Kamal, Naglaa M., Saadah, Omar I., Alheraiti, Shahad S., Attar, Ruwayd, Alsufyani, Asmaa D., El-Shabrawi, Moratda H.F., Sherief, Laila M.

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First report of SYNE1 arthrogryposis multiplex congenita from Saudi Arabia with a novel mutation: a case report von Kamal, Naglaa M., Alzeky, AlaaEddin M., Omair, Maher R., Attar, Ruwayd A., Alotaibi, Abdullah M., Safar, Abdullah, Alosaimi, Nawal S., Abosabie, Sara A. S.

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Facial Asymmetry in a Newly Born Baby: Diagnostic Challenge von Kamal, Naglaa M, Omair, Maher MR, Attar, Ruwayd, Abosabie, Salma AS, Asiri, Nawras M, Sherief, Laila M, El-Shabrawi, Mortada

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Pyridoxine Refractory Sideroblastic Anemia: Diagnosis and Misdiagnosis von Alam, Muhammad Matloob, Alathaibi, Abdulrhman, Attar, Ruwayd Adel, Kashif, Muhammad, Al-Ghamdi, Hamdan Saeed, Alharthi, Sultan Abdulaziz, Bokhary, Abdulmohsen, Althomali, Muteb

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Facial Asymmetry in a Newly Born Baby: Diagnostic Challenge von Kamal, Naglaa M, Omair, Maher Mr, Attar, Ruwayd, Abosabie, Salma As, Asiri, Nawras M, Sherief, Laila M, El-Shabrawi, Mortada

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