National screening for developmental delays and their determinants among Egyptian school age children: A step towards implementing life skills programs von Metwally, Ammal M, Nassar, Maysa S, Salah El-Din, Ebtissam M, Abdallah, Ali M, Khadr, Zeinab, Abouelnaga, Marwa W, Ashaat, Engy A, El-Saied, Mostafa M, Elwan, Ahmed M, Bassiouni, Randa I, Monir, Zeinab M, Badawy, Hala Y, Dewdar, Eman M, El-Hariri, Hazem M, Aboulghate, Ahmed, Hanna, Carine, Rabah, Thanaa M, Mohsen, Amira, Elabd, Mona A

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A national screening for the prevalence and profile of disability types among Egyptian children aged 6–12 years: a community-based population study von Metwally, Ammal M, Salah El-Din, Ebtissam M, Abdel-Latif, Ghada A, Nagi, Dina A, El Etreby, Lobna A, Abdallah, Ali M, Khadr, Zeinab, Bassiouni, Randa I, Abdel Raouf, Ehab R, Elsaied, Amal, Elkhatib, Alshaimaa A, Sallam, Sara F, El-Sonbaty, Marwa M, Shehata, Manal A, Elghareeb, Nahed A, Badawy, Hala Y, Ahmed, Doaa E, Ibrahim, Nihad A, Emam, Hanaa, Abd El Dayem, Soha M, Fathy, Asmaa M

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National screening for Egyptian children aged 1 year up to 12 years at high risk of Autism and its determinants: a step for determining what ASD surveillance needs von Metwally, Ammal M, Helmy, Mona A, Salah El-Din, Ebtissam M, Saleh, Rehan M, Abdel Raouf, Ehab R, Abdallah, Ali M, Khadr, Zeinab, Elsaied, Amal, El-Saied, Mostafa M, Bassiouni, Randa I, Nagi, Dina A, Shehata, Manal A, El-Alameey, Inas R, El-Hariri, Hazem M, Salama, Somia I, Rabah, Thanaa M, Abdel-Latif, Ghada A, El Etreby, Lobna A, Elmosalami, Dalia M, Sami, Samia M, Eltahlawy, Eman, Ibrahim, Nihad A, Elghareeb, Nahed A, Badawy, Hala Y, Dewdar, Eman M, Ashaat, Engy A

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Novel compound heterozygous mutations in MCPH1 gene causes primary microcephaly in Saudi family von Naseer, Muhammad I, Rasool, Mahmood, Abdulkareem, Angham A, Bassiouni, Randa I, Algahtani, Hussein, Chaudhary, Adeel G, Al-Qahtani, Mohammad H

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Molecular Diagnosis of Fragile X Syndrome Using Methylation Sensitive Techniques in a Cohort of Patients With Intellectual Disability von Chaudhary, Adeel G., PhD, Hussein, Ibtessam R., MD PhD, Abuzenadah, Adel, PhD, Gari, Mamdouh, PhD, Bassiouni, Randa, MD, PhD, Sogaty, Samira, MBBCh, Lary, Sahira, PhD, Al-Quaiti, Maha, MSc, Al Balwi, Mohammed, PhD, Al Qahtani, Mohammed, PhD

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The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes von Monies, Dorota, Abouelhoda, Mohamed, AlSayed, Moeenaldeen, Alhassnan, Zuhair, Alotaibi, Maha, Al-Owain, Mohammed, Shah, Ayaz, Rahbeeni, Zuhair, Al-Muhaizea, Mohammad A., Alzaidan, Hamad I., Cupler, Edward, Bohlega, Saeed, Faqeih, Eissa, Faden, Maha, Alyounes, Banan, Jaroudi, Dyala, Goljan, Ewa, Elbardisy, Hadeel, Akilan, Asma, Albar, Renad, Aldhalaan, Hesham, Gulab, Shamshad, Chedrawi, Aziza, Al Saud, Bandar K, Kurdi, Wesam, Makhseed, Nawal, Alqasim, Tahani, El Khashab, Heba Y., Al-Mousa, Hamoud, Kanaan, Imaduddin, Algoufi, Talal, Alsaleem, Khalid, Basha, Talal A., Al-Murshedi, Fathiya, Al-Kindy, Adila, Al-Hajjar, Sami, Alyamani, Suad, Aldhekri, Hasan, Al-Mehaidib, Ali, Arnaout, Rand, Dabbagh, Omar, Shagrani, Mohammad, Broering, Dieter, Alqassmi, Amal, Almugbel, Maisoon, AlQuaiz, Mohammed, Alsaman, Abdulaziz, Al-Thihli, Khalid, Sulaiman, Raashda A., Al-Dekhail, Wajeeh, Alsaegh, Abeer, Bashiri, Fahad A., Qari, Alya, Alhomadi, Suzan, Alkuraya, Hisham, Alsebayel, Mohammed, Hamad, Muddathir H, Szonyi, Laszlo, Abaalkhail, Faisal, Al-Mayouf, Sulaiman M., Almojalli, Hamad, Alqadi, Khalid S., Elsiesy, Hussien, Shuaib, Taghreed M., Seidahmed, Mohammed Zain, Abosoudah, Ibraheem, Akleh, Hana, AlGhonaium, Abdulaziz, Alkharfy, Turki M., Al Mutairi, Fuad, Eyaid, Wafa, Alshanbary, Abdullah, Sheikh, Farrukh R., Alsohaibani, Fahad I., Al Tala, Saeed, Balkhy, Soher, Bassiouni, Randa, Alenizi, Ahmed S., Hussein, Maged H., Hassan, Saeed, Khalil, Mohamed, Tabarki, Brahim, Alshahwan, Saad, Oshi, Amira, Sabr, Yasser, Alsaadoun, Saad, Salih, Mustafa A., Mohamed, Sarar, Sultana, Habiba, Tamim, Abdullah, El-Haj, Moayad, Alshahrani, Saif, Bubshait, Dalal K., Alfadhel, Majid, Faquih, Tariq, El-Kalioby, Mohamed, Shah, Zeeshan, Moghrabi, Nabil, Meyer, Brian F., Alkuraya, Fowzan S.

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Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects von Hussein, Ibtessam R., Bader, Rima S., Chaudhary, Adeel G., Bassiouni, Randa, Alquaiti, Maha, Ashgan, Fai, Schulten, Hans-Juergen, Al Qahtani, Mohammad H.

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The Effect of Diet on Antioxidant Status in Patients with Galactosemia von ., Hala T. El-Bassyouni, ., Adel M. Ashour, ., Afaf Ezzat, ., Randa Bassiouni, ., Ekram M. Fateen

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Application of array comparative genomic hybridization (array- CGH) for detection of chromosomal imbalances in children with developmental delay/congenital malformations in Saudi A... von Hussein, Ibtessam Ramzi, Chaudhary, Adeel G, Bassiouni, Randa, AlQuaiti, Maha, Sogaty, Samira, Al-Qahtani, Mohammed

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National screening for developmental delays and their determinants among Egyptian school age children: A step towards implementing life skills programs von Ammal M. Metwally, Maysa S. Nassar, Ebtissam M. Salah El-Din, Ali M. Abdallah, Zeinab Khadr, Marwa W. Abouelnaga, Engy A. Ashaat, Mostafa M. El-Saied, Ahmed M. Elwan, Randa I. Bassiouni, Zeinab M. Monir, Hala Y. Badawy, Eman M. Dewdar, Hazem M. El-Hariri, Ahmed Aboulghate, Carine Hanna, Thanaa M. Rabah, Amira Mohsen, Mona A. Elabd

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Mutational Analysis of the alpha-L-iduronidase gene in three Egyptian families: identification of three novel mutations and five novel polymorphisms von Amr, Khalda, Katoury, Ahmed, Abdel-Hamid, Mohamed, Bassiouni, Randa, Ibrahim, Mona, Fateen, Ekram

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Sensitivity of DCSR3/GAPDH Ratio Using Quantitative Real-Time PCR in the Rapid Prenatal Diagnosis for Down Syndrome von Helmy, Sanaa M.H., Ismail, Somaya, Bassiouni, Randa, Gaber, Khaled R.

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Additional file 2 of National screening for Egyptian children aged 1 year up to 12 years at high risk of Autism and its determinants: a step for determining what ASD surveillance n... von Metwally, Ammal M., Helmy, Mona A., Salah El-Din, Ebtissam M., Saleh, Rehan M., Abdel Raouf, Ehab R., Abdallah, Ali M., Khadr, Zeinab, Elsaied, Amal, El-Saied, Mostafa M., Bassiouni, Randa I., Nagi, Dina A., Shehata, Manal A., El-Alameey, Inas R., El-Hariri, Hazem M., Salama, Somia I., Rabah, Thanaa M., Abdel-Latif, Ghada A., El Etreby, Lobna A., Elmosalami, Dalia M., Sami, Samia M., Eltahlawy, Eman, Ibrahim, Nihad A., Elghareeb, Nahed A., Badawy, Hala Y., Dewdar, Eman M., Ashaat, Engy A.

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Additional file 1 of A national screening for the prevalence and profile of disability types among Egyptian children aged 6–12 years: a community-based population study von Metwally, Ammal M., Salah El-Din, Ebtissam M., Abdel-Latif, Ghada A., Nagi, Dina A., El Etreby, Lobna A., Abdallah, Ali M., Khadr, Zeinab, Bassiouni, Randa I., Abdel Raouf, Ehab R., Elsaied, Amal, Elkhatib, Alshaimaa A., Sallam, Sara F., El-Sonbaty, Marwa M., Shehata, Manal A., Elghareeb, Nahed A., Badawy, Hala Y., Ahmed, Doaa E., Ibrahim, Nihad A., Emam, Hanaa, Abd El Dayem, Soha M., Fathy, Asmaa M.

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