The Molecular Genetics of Congenital Idiopathic Nystagmus
Author:
Publisher
Informa UK Limited
Subject
Ophthalmology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/08820530600614017
Reference18 articles.
1. Congenital Motor Nystagmus Linked to Xq26-q27
2. Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12
3. A Gene for X-Linked Idiopathic Congenital Nystagmus (NYS1) Maps to Chromosome Xp11.4-p11.3
4. Exclusion of Chromosome Regions 6p12 and 15q11, but Not Chromosome Region 7p11, in a German Family with Autosomal Dominant Congenital Nystagmus
5. Congenital nystagmus cosegregating with a balanced 7;15 translocation.
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1. Ocular findings and genomics of X-linked recessive disorders: A review;Indian Journal of Ophthalmology;2022
2. A new gene mutation in a family with idiopathic infantile nystagmus;Saudi Journal of Ophthalmology;2021
3. Ophthalmic genetics practice and research in India: Vision in 2020;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2020-08-31
4. Nystagmus in the Child with Congenital Cataract;Congenital Cataract;2016-10-15
5. Molecular genetic analysis of patients with sporadic and X-linked infantile nystagmus;BMJ Open;2016-04
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