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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, FRCP
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Altaf 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
PhD
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Ali 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
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Thomas 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
MD
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Arif 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
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Article Information

vol. 21 no. 1 72-74
DOI 
https://doi.org/10.17712/nsj.2016.1.20150098
PubMed 
26818173

Published By 
Neurosciences Journal
Online ISSN 
1658-3183
History 
  • Received February 3, 2015
  • Accepted August 26, 2015
  • Published online November 13, 2020.

Copyright & Usage 
Copyright: © Neurosciences Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work.

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Neurosciences Journal: 21 (1)
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Vol. 21, Issue 1
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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

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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
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© 2025 Neurosciences Journal Neurosciences is copyright under the Berne Convention and the International Copyright Convention. All rights reserved. Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3183. Print ISSN 1319-6138.

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