Congenital Ectropion Uvea and Mechanisms of Glaucoma in Neurofibromatosis Type 1:
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
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3. Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus;Viskochil;Cell,1990
4. Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis;Menon;Proc Natl Acad Sci U S A,1990
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