DETECTION OF THE CARRIER STATE FOR AN X-LINKED DISORDER, THE LESCH-NYHAN SYNDROME, BY THE USE OF LYMPHOCYTE CLONING

被引：43
作者：
DEMPSEY, JL
MORLEY, AA
SESHADRI, RS
EMMERSON, BT
GORDON, R
BHAGAT, CI
机构：
[1] FLINDERS UNIV S AUSTRALIA,MED CTR,DEPT HAEMATOL,BEDFORD PK,SA 5042,AUSTRALIA
[2] PRINCESS ALEXANDRA HOSP,DEPT MED,BRISBANE,AUSTRALIA
[3] QUEEN ELIZABETH II MED CTR,DEPT CLIN BIOCHEM,PERTH,AUSTRALIA
来源：
HUMAN GENETICS | 1983年 / 64卷 / 03期
关键词：
D O I：
10.1007/BF00279414
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：288 / 290
页数：3
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