作者：
Al-Owain,M. [1]
;
Imtiaz,F. [2]
;
Shuaib,T. [3]
;
Edrees,A. [4]
;
Al-Amoudi,M. [5]
;
Sakati,N. [6]
;
Al-Hassnan,Z. [7]
;
Bamashmous,H. [8]
;
Rahbeeni,Z. ;
Al-Ameer,S. ;
Faqeih,E. ;
Meyer,B. ;
Al-Hashem,A. ;
Garout,W. ;
Al-Odaib,A. ;
Rashed,M. ;
Al-Aama,J.Y.
作者单位：
Department of Pediatrics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
[1]
Department of Medical Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi
[2]
Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
[3]
Pharmagene Laboratory, Giza, Egypt
[4]
Princess Al-Jawhara Center of Excellence in Research of Hereditary Disorders, King Abdulaziz
[5]
Department of Pediatrics, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia
[6]
Department of Pediatrics, King Fahad Medical City, Riyadh, Saudi Arabia
[7]
Department of Pediatrics, Armed Forces Hospital, Riyadh, Saudi Arabia
[8]
发布时间
2018-08-24
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