Partial monosomy 10p syndrome.
作者信息
Koenig R, Kessel E, Schoenberger W
出版信息
Ann Genet. 1985;28(3):173-6.
PMID: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.
摘要
Zotero 插件