Regional fine mapping of the β crystallin genes on chromosome 22 excludes these genes as physically linked markers for neurofibromatosis type 2
Author:
Publisher
Wiley
Subject
Cancer Research,Genetics
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1. Functional Annotation of Proteome Encoded by Human Chromosome 22;Journal of Proteome Research;2014-04-29
2. An informative Hindlll polymorphism associated with the βB1 crystallin gene (CRYBB1) on human chromosome 22;Clinical Genetics;2008-04-23
3. Congenital cataracts: gene mapping;Human Genetics;2000-01-31
4. Characterization of the human synaptogyrin gene family;Human Genetics;1998-09-02
5. Blindness, deafness, quadriparesis, and a retinal malformation: the ravages of neurofibromatosis 2;Survey of Ophthalmology;1996-09
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