%0 Journal Article
%T Genetical Investigation on a Rare Genealogy of Congenital Camptodactyly<br>一个罕见的屈指畸形家系的遗传学调查
%A Feng Xia
%A Yong-jun Cao
%A Zong-yuan Hong
%A Mei-ying Li
%A Shao-qing Ding
%A <br>夏峰
%A 曹勇军
%A 洪宗元
%A 李美英
%A 丁绍青
%J 遗传
%D 2002
%I 
%X 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.
%K congenital camptodactyly
%K inherited disease<br>屈指畸形家系
%K 遗传学调查
%K 遗传性疾病
%U http://www.alljournals.cn/get_abstract_url.aspx?pcid=90BA3D13E7F3BC869AC96FB3DA594E3FE34FBF7B8BC0E591&jid=3E23F50E071DF18E21B2F5AEE4F1FA5E&aid=AB196F2E31A1393C&yid=C3ACC247184A22C1&vid=B91E8C6D6FE990DB&iid=B31275AF3241DB2D&sid=6C62BFE34266FA92&eid=421C41B8FD4D3EBA&journal_id=0253-9772&journal_name=遗传&referenced_num=0&reference_num=7