المؤلفون: AlSaman, Abdulaziz S., Al Ghamdi, Fouad, Bamaga, Ahmed K., AlShaikh, Nahla, Al Muqbil, Mohammed, Muthaffar, Osama, Bashiri, Fahad A., Ali, Baleegh, Mulayim, Arzu, Heider, Elena, Alshahrani, Abdullah A., Al Muhaizea, Mohammed A.

المساهمون: PTC Therapeutics

المصدر: Frontiers in Pediatrics ; volume 10 ; ISSN 2296-2360

مصطلحات موضوعية: Pediatrics, Perinatology and Child Health

الإتاحة: https://doi.org/10.3389/fped.2022.1020059Test

المؤلفون: Al‐Muhaizea, Mohammed A., Aldeeb, Hanouf, Almass, Rawan, Jaber, Hadeel, Binhumaid, Felwa, Alquait, Laila, Abukhalid, Musaad, Aldhalaan, Hesham, Alsagob, Maysoon, Al‐Bakheet, Albandary, Aldosary, Mazhor, Alkofide, Hadeel, Alrasheed, Maha M., Colak, Dilek, Kaya, Namik

المصدر: Annals of Human Genetics ; volume 86, issue 1, page 34-44 ; ISSN 0003-4800 1469-1809

الإتاحة: https://doi.org/10.1111/ahg.12445Test

المؤلفون: Al‐Muhaizea, Mohammed A.¹ (AUTHOR), Aldeeb, Hanouf^2,3,4 (AUTHOR), Almass, Rawan^3,5 (AUTHOR), Jaber, Hadeel^3,4 (AUTHOR), Binhumaid, Felwa³ (AUTHOR), Alquait, Laila^2,3 (AUTHOR), Abukhalid, Musaad¹ (AUTHOR), Aldhalaan, Hesham¹ (AUTHOR), Alsagob, Maysoon^3,6 (AUTHOR), Al‐Bakheet, Albandary^2,3 (AUTHOR), Aldosary, Mazhor^2,3 (AUTHOR), Alkofide, Hadeel⁴ (AUTHOR), Alrasheed, Maha M.⁴ (AUTHOR), Colak, Dilek⁷ (AUTHOR), Kaya, Namik^2,3 (AUTHOR) nkaya@kfshrc.edu.sa

المصدر: Annals of Human Genetics. Jan2022, Vol. 86 Issue 1, p34-44. 11p.

مصطلحات موضوعية: *ATAXIA telangiectasia, *GENETIC variation, *CONSANGUINITY, *GENETICS, *GENETIC counseling, *MOVEMENT disorders

مصطلحات جغرافية: SAUDI Arabia

المؤلفون: El-Hattab, Ayman W, Dai, Hongzheng, Almannai, Mohammed, Wang, Julia, Faqeih, Eissa A, Al Asmari, Ali, Saleh, Mohammed A M, Elamin, Mohammed A O, Alfadhel, Majid, Alkuraya, Fowzan S, Hashem, Mais, Aldosary, Mazhor S, Almass, Rawan, Almutairi, Faten B, Alsagob, Maysoon, Al-Owain, Mohammed, Al-Sharfa, Shirin, Al-Hassnan, Zuhair N, Rahbeeni, Zuhair, Al-Muhaizea, Mohammed A, Makhseed, Nawal, Foskett, Gretchen K, Stevenson, David A, Gomez-Ospina, Natalia, Lee, Chung, Boles, Richard G, Schrier Vergano, Samantha A, Wortmann, Saskia B, Sperl, Wolfgang, Opladen, Thomas, Hoffmann, Georg F, Hempel, Maja, Prokisch, Holger, Alhaddad, Bader, Mayr, Johannes A, Chan, Wenyaw, Kaya, Namik, Wong, Lee-Jun C

المساهمون: Institut für Humangenetik

مصطلحات موضوعية: info:eu-repo/classification/ddc

العلاقة: https://mediatum.ub.tum.de/1441666Test

الإتاحة: https://doi.org/10.1002/humu.23341Test
https://mediatum.ub.tum.de/1441666Test

المؤلفون: El-Hattab, Ayman W., Dai, Hongzheng, Almannai, Mohammed, Wang, Julia, Faqeih, Eissa A., Al Asmari, Ali, Saleh, Mohammed A. M., Elamin, Mohammed A. O., Alfadhel, Majid, Alkuraya, Fowzan S., Hashem, Mais, Aldosary, Mazhor S., Almass, Rawan, Almutairi, Faten B., Alsagob, Maysoon, Al-Owain, Mohammed, Al-Sharfa, Shirin, Al-Hassnan, Zuhair N., Rahbeeni, Zuhair, Al-Muhaizea, Mohammed A.

المصدر: Human Mutation; Dec2017, Vol. 38 Issue 12, p1649-1659, 11p

المؤلفون: Al‐Owain, Mohammed, Al‐Hashem, Amal, Al‐Muhaizea, Mohammed, Humaidan, Hani, Al‐Hindi, Hindi, Al‐Homoud, Iftetah, Al‐Mogarri, Ibrahim

المصدر: American Journal of Medical Genetics Part A ; volume 152A, issue 7, page 1849-1853 ; ISSN 1552-4825 1552-4833

الإتاحة: https://doi.org/10.1002/ajmg.a.33421Test