OtherClinical Note
Open Access
Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder
Khaled K. Abu-Amero, Altaf A. Kondkar, Ali M. Hellani, Thomas M. Bosley and Arif O. Khan
Neurosciences Journal January 2016, 21 (1) 72-74; DOI: https://doi.org/10.17712/nsj.2016.1.20150098
Khaled K. Abu-Amero
From the Department of Ophthalmology (Abu-Amero, Kondkar, Bosley), the Glaucoma Research Chair (Abu-Amero, Kondkar), College of Medicine, King Saud University, the Division of Pediatric Ophthalmology (Khan), King Khaled Eye Specialist Hospital, Riyadh, Kingdom of Saudi Arabia, and the Viafet Genomic Center (Hellani), Sydney, Australia, and the Department of Ophthalmology (Abu-Amero), College of Medicine, Jacksonville, Florida, USA
PhD, FRCPAltaf A. Kondkar
From the Department of Ophthalmology (Abu-Amero, Kondkar, Bosley), the Glaucoma Research Chair (Abu-Amero, Kondkar), College of Medicine, King Saud University, the Division of Pediatric Ophthalmology (Khan), King Khaled Eye Specialist Hospital, Riyadh, Kingdom of Saudi Arabia, and the Viafet Genomic Center (Hellani), Sydney, Australia, and the Department of Ophthalmology (Abu-Amero), College of Medicine, Jacksonville, Florida, USA
PhDAli M. Hellani
From the Department of Ophthalmology (Abu-Amero, Kondkar, Bosley), the Glaucoma Research Chair (Abu-Amero, Kondkar), College of Medicine, King Saud University, the Division of Pediatric Ophthalmology (Khan), King Khaled Eye Specialist Hospital, Riyadh, Kingdom of Saudi Arabia, and the Viafet Genomic Center (Hellani), Sydney, Australia, and the Department of Ophthalmology (Abu-Amero), College of Medicine, Jacksonville, Florida, USA
PhDThomas M. Bosley
From the Department of Ophthalmology (Abu-Amero, Kondkar, Bosley), the Glaucoma Research Chair (Abu-Amero, Kondkar), College of Medicine, King Saud University, the Division of Pediatric Ophthalmology (Khan), King Khaled Eye Specialist Hospital, Riyadh, Kingdom of Saudi Arabia, and the Viafet Genomic Center (Hellani), Sydney, Australia, and the Department of Ophthalmology (Abu-Amero), College of Medicine, Jacksonville, Florida, USA
MDArif O. Khan
From the Department of Ophthalmology (Abu-Amero, Kondkar, Bosley), the Glaucoma Research Chair (Abu-Amero, Kondkar), College of Medicine, King Saud University, the Division of Pediatric Ophthalmology (Khan), King Khaled Eye Specialist Hospital, Riyadh, Kingdom of Saudi Arabia, and the Viafet Genomic Center (Hellani), Sydney, Australia, and the Department of Ophthalmology (Abu-Amero), College of Medicine, Jacksonville, Florida, USA
MD
Submit a Response to This Article
Jump to comment:
No eLetters have been published for this article.
In this issue
Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder
Khaled K. Abu-Amero, Altaf A. Kondkar, Ali M. Hellani, Thomas M. Bosley, Arif O. Khan
Neurosciences Journal Jan 2016, 21 (1) 72-74; DOI: 10.17712/nsj.2016.1.20150098
Jump to section
Related Articles
- No related articles found.
Cited By...
- No citing articles found.