Ocular manifestations in the X-linked intellectual disability syndromes-Reference-Cited by-同舟云学术

Ocular manifestations in the X-linked intellectual disability syndromes

Published:2017-01-23 Issue:5 Volume:38 Page:401-412
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Couser Natario L.¹²^ORCID,Masood Maheer M.³,Aylsworth Arthur S.²⁴,Stevenson Roger E.⁵

Affiliation:

1. Department of Ophthalmology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA

2. Division of Genetics and Metabolism, Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA

3. University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA

4. Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA

5. Greenwood Genetic Center, JC Self Research Institute of Human Genetics, Greenwood, South Carolina, USA

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2016.1247459

Reference72 articles.

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4. Dyskeratosis congenita: delay in diagnosis and successful treatment of pancytopenia by bone marrow transplantation

5. Wijker M, Ligtenberg MJ, Schoute F, et al. The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region . Am J Hum Genet 1995;56:1096–1100.

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