The 6p25 deletion syndrome: An update on a rare neurocristopathy-Reference-Cited by-同舟云学术

The 6p25 deletion syndrome: An update on a rare neurocristopathy

Published:2016-04-12 Issue:2 Volume:38 Page:101-107
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

de Vos Ivo J. H. M.¹,Stegmann Alexander P. A.¹,Webers Carroll A. B.²,Stumpel Constance T. R. M.¹

Affiliation:

1. Department of Clinical Genetics and School for Oncology and Developmental Biology (GROW), Maastricht University Medical Center+, Maastricht, the Netherlands

2. Department of Ophthalmology, Maastricht University Medical Center+, Maastricht, the Netherlands

Funder

Agency for Science, Technology and Research

Publisher

Informa UK Limited

Subject

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

Link

https://tandfonline.com/doi/pdf/10.3109/13816810.2016.1164191

Reference36 articles.

1. A Review of Anterior Segment Dysgeneses

2. Axenfeld-Rieger syndrome in the age of molecular genetics

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4. Current molecular understanding of Axenfeld–Rieger syndrome

5. The Axenfeld syndrome and the Rieger syndrome.

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