Genetical Investigation on a Rare Genealogy of Congenital Camptodactyly
一个罕见的屈指畸形家系的遗传学调查

Introduced a rare genealogy of autosomal dominant inheritance disease, which cardinal signs were congenital camptodactyly and functional disturbance of the proximal interphalangeal joints of the II, III, IV, V fingers. Part cases had congenital high myopia.