Hereditary deletion of the entire FAM20C gene in a patient with Raine syndrome-Reference-Cited by-同舟云学术

Hereditary deletion of the entire FAM20C gene in a patient with Raine syndrome

Author:

Ababneh Farouq K.¹,AlSwaid Abdulrahman¹,Youssef Talaat²,Al Azzawi Manaf³,Crosby Andrew⁴,AlBalwi Mohammed A.⁵⁶⁷

Affiliation:

1. Division of Genetics; Department of Pediatrics; King Abdulaziz Medical City for National Guard Health Affairs; Riyadh Saudi Arabia

2. Department of Radiology; King Abdulaziz Medical City for National Guard Health Affairs; Riyadh Saudi Arabia

3. Division of Plastic and Craniofacial Surgery; King Abdulaziz Medical City for National Guard Health Affairs; Riyadh Saudi Arabia

4. Medical Genetics; St. George's University; London UK

5. Department of Pathology and Laboratory Medicine; King Abdulaziz Medical City for National Guard Health Affairs; Riyadh Saudi Arabia

6. College of Medicine; King Saud Bin Abdulaziz University for Health Sciences; Riyadh Saudi Arabia

7. Medical Biotechnology; King Abdullah International Medical Research Center; National Guard Health Affairs; Riyadh Saudi Arabia

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference22 articles.

Cited by 35 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献