Progress in genetics of coronary artery disease by Radwa Gamal

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Congenital hypothyroidism: a case report of an Egyptian child with congenital heart disease, pelvic kidney and cavernous transformation of portal vein by Heba Elsedfy, Radwa Gamal

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Meier–Gorlin syndrome: An additional Egyptian patient with gastroesophageal reflux, hydronephrosis, renal stones and hypoplastic labia majora and minora with clitromegaly by Rabah M. Shawky, Radwa Gamal

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Removal notice to “An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings” [Egypt J Med Hum Genet 18 (2017) 393–396] by Solaf M. Elsayed, Radwa Gamal

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TEMPORARY REMOVAL: An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings by Solaf M. Elsayed, Radwa Gamal

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C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot’s spots and agenesis of the corpus callosum in an Egyptian child by Rabah M. Shawky, Radwa Gamal

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Cantu syndrome in an Egyptian child by Rabah M. Shawky, Radwa Gamal

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THE ATMOSPHERIC ELEMENTS OF THE EGYPTIAN MUSEUMS AND THEIR EFFECT ON THE EGYPTIANS' INTENTIONS TO REVISIT by Radwa GAMAL, Jermin ABDELKAFY, Dalia SOLIMAN

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Berardinelli–Seip syndrome type 2 – An Egyptian child by Rabah M. Shawky, Radwa Gamal, Neveen S Seifeldin

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Blepharophimosis, ptosis, epicanthus inversus syndrome type 2 with red hair, lymphedema of lower limbs and kidney stones in an Egyptian patient by Rabah M. Shawky, Radwa Gamal, Neveen S. Seifeldin

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Kabuki make-up syndrome with genitourinary anomalies, ophthalmologic features and hyperpigmentation in an Egyptian child by Rabah M. Shawky, Radwa Gamal, Nayera Mostafa

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Moebius syndrome with macular hyperpigmentation, skeletal anomalies, and hypoplasia of pectoralis major muscle in an Egyptian child by Rabah M. Shawky, Radwa Gamal, Shaimaa Abdelsattar Mohammad

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Baraitser–Winter syndrome: An additional Egyptian patient with skeletal anomalies, bilateral iris and choroid colobomas, retinal hypoplasia and hypoplastic scrotum by Rabah M. Shawky, Radwa Gamal, Shaimaa Abdelsattar Mohammad

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The interactive digital direction in the interior design of libraries by Radwa Gamal, Asmaa hamed, Hussein Kamel El-Nabawi

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Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II by Rabah M. Shawky, Radwa Gamal, Shaimaa Abdelsattar Mohammad

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Challenges in diagnosis and counseling of a family with two recessive neurometabolic disorders by Heba S. Abd-Elkhalek, Radwa Gamal, Osama K. Zaki, Solaf M. Elsayed

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The value of simultaneous determination of blood large neutral amino acids and tetrahydrobiopterin metabolites in the diagnosis of atypical hyperphenylalaninemia by Nadia Salama, Gamalte Elgedawy, Radwa Gamal, Osama Zaki, Ashraf Khalil, Manar Obada

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Currarino Triad: Importance of Preoperative Magnetic Resonance Imaging by Amr AbdelHamid AbouZeid, Shaimaa Abdelsattar Mohammad, Mohammad Seada, Khaled Khiamy, Radwa Gamal

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Neurofibromatosis type 1 and multiple sclerosis: Genetically related diseases by Solaf M. Elsayed, Nagia Fahmy, Radwa Gamal, Mohamed Wafik, Dina Zamzam, Mai Fahmy, Mahmoud Suelam

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Oral–Facial–Digital Syndrome type VI with self mutilations by Rabah M. Shawky, Heba Salah Abd-Elkhalek Elabd, Shaimaa Gad, Radwa Gamal, Shaimaa Abdelsattar Mohammad

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