The Usher syndromes
Author:
Affiliation:
1. Department of Biometry and Genetics, LSU Medical Center, 1901 Perdido Street, New Orleans, LA 70112
Publisher
Wiley
Subject
Genetics (clinical)
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/%28SICI%291096-8628%2819990924%2989%3A3%3C158%3A%3AAID-AJMG6%3E3.0.CO%3B2-%23
Reference110 articles.
1. Mutation Profile of All 49 Exons of the Human Myosin VIIA Gene, and Haplotype Analysis, in Usher 1B Families from Diverse Origins
2. Increased incidence of abnormal nasal cilia in patients with retinitis pigmentosa
3. Fine mapping of the Usher syndrome type IC to chromosome 11p14 and identification of flanking markers by haplotype analysis;Ayyagari R;Molecular Vision,1995
4. Construction of a YAC contig encompassing the Usher syndrome type 1C and familial hyperinsulinism loci on chromosome 11p14-15.1.
5. Decreased content of docosahexaenoate and arachidonate in plasma phospholipids in usher's syndrome
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