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Title: Partial monosomy 10p syndrome. Author: Koenig R, Kessel E, Schoenberger W. Journal: Ann Genet; 1985; 28(3):173-6. PubMed ID: 3879152. Abstract: A newborn infant with monosomy 10p13 is reported. The clinical signs and symptoms of the present case are compared with those of previously described cases. Although there is no pathognomonic feature, a characteristic monosomy 10p syndrome is recognizable.[Abstract] [Full Text] [Related] [New Search]