Genetic investigation of 93 families with microphthalmia or posterior microphthalmos

Author:

Patel N.1,Khan A.O.12,Alsahli S.1,Abdel-Salam G.3,Nowilaty S.R.4,Mansour A.M.5,Nabil A.6,Al-Owain M.78,Sogati S.9,Salih M.A.10,Kamal A.M.11,Alsharif H.1,Alsaif H.S.1,Alzahrani S.S.1,Abdulwahab F.1,Ibrahim N.1,Hashem M.1,Faquih T.112,Shah Z.A.112,Abouelhoda M.112,Monies D.112,Dasouki M.1,Shaheen R.1,Wakil S.M.1,Aldahmesh M.A.1,Alkuraya F.S.1128ORCID

Affiliation:

1. Department of Genetics; King Faisal Specialist Hospital and Research Center; Riyadh 11211 Saudi Arabia

2. Eye Institute, Cleveland Clinic Abu Dhabi; Abu Dhabi United Arab Emirates

3. National Research Center; Cairo Egypt

4. Vitreo-retinal Division; King Khaled Eye Specialist Hospital; Riyadh Saudi Arabia

5. Department of Ophthalmology; American University of Beirut; Beirut Lebanon

6. Human Genetics Department, Medical Research Institute; Alexandria University; Alexandria Egypt

7. Department of Medical Genetics; King Faisal Specialist Hospital and Research Center; Riyadh Saudi Arabia

8. Department of Anatomy and Cell Biology; College of Medicine, Alfaisal University; Riyadh Saudi Arabia

9. Department of Medical Genetics; King Fahad General Hospital; Jeddah Saudi Arabia

10. Division of Pediatrics Neurology; College of Medicine, King Saud University; Riyadh Saudi Arabia

11. Department of Ophthalmology; Cairo University; Cairo Egypt

12. Saudi Human Genome Project; King Abdulaziz City for Science and Technology; Riyadh Saudi Arabia

Funder

King Salman Center for Disability Research

Saudi Human Genome Program

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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