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Ophthalmology, ISSN 0161-6420, 2008, Volume 115, Issue 6, pp. 975 - e1
Journal Article
British Journal of Ophthalmology, ISSN 0007-1161, 05/2016, Volume 100, Issue 5, pp. 601 - 606
Journal Article
Journal Article
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 07/2012, Volume 154, Issue 1, pp. 210 - 211
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 07/2012, Volume 154, Issue 1, pp. 210 - 211
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 07/2012, Volume 154, Issue 1, p. 210
  Because corneal involvement may be more immediately sight-threatening than lid involvement, we also believed it appropriate to grade overall disease... 
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 07/2012, Volume 154, Issue 1, pp. 210 - 211
Journal Article
Investigative Ophthalmology & Visual Science, ISSN 0146-0404, 10/2002, Volume 43, Issue 10, pp. 3174 - 3180
Journal Article
American Journal of Ophthalmology, ISSN 0002-9394, 2012, Volume 154, Issue 1, pp. 210 - 211
Journal Article
2010, ISBN 9812832971, xxvi, 390
Book
Human mutation, 2007, Volume 28, Issue 5, pp. 522 - 523
Autosomal recessive congenital hereditary endothelial dystrophy (CHED2) is a severe and rare corneal disorder that presents at birth or shortly thereafter,... 
Corneal Diseases - genetics | United States | Humans | Antiporters - genetics | Mutation | Genes, Recessive | Anion Transport Proteins - genetics | Genetic Carrier Screening | India | Index Medicus
Journal Article
Annals of the Academy of Medicine Singapore, ISSN 0304-4602, 06/2006, Volume 35, Issue 6, pp. 400 - 407
Journal Article
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