Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?
published in: Genes, Chromosomes and Cancer
date of publication: 1999-06-01
main subject: neurofibromatosis type II, phenotype
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Article - wd:Q77780271