Dyskeratosis Congenita and Familial Pancytopenia

Volume: 192, Issue: 3, Pages: 203 - 203
Published: Apr 19, 1965
Abstract
Four or possibly five males in a kinship group had features of dyskeratosis congenita, a syndrome comprising poikiloderma atrophicans vasculare, dystrophia unguium, and leukoplakia oris. In addition, three members of the kinship demonstrated hematologic changes compatible with the hypoplastic anemia described by Fanconi. Based on the hemopoietic disturbance found in these three cases and that observed in seven similar cases from the literature,...
Paper Details
Title
Dyskeratosis Congenita and Familial Pancytopenia
Published Date
Apr 19, 1965
Journal
Volume
192
Issue
3
Pages
203 - 203
Citation AnalysisPro
  • Scinapse’s Top 10 Citation Journals & Affiliations graph reveals the quality and authenticity of citations received by a paper.
  • Discover whether citations have been inflated due to self-citations, or if citations include institutional bias.