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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