ASSOCIATIONS BETWEEN RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS DETECTED WITH A PROBE FOR HUMAN 21-HYDROXYLASE (21-OH) AND 2 CLINICAL FORMS OF 21-OH DEFICIENCY

被引:29
作者
MORNET, E
COUILLIN, P
KUTTEN, F
RAUX, MC
WHITE, PC
COHEN, D
BOUE, A
DAUSSET, J
机构
[1] INST NATL RECH MED,UNITE 73,F-75016 PARIS,FRANCE
[2] HOP NECKER ENFANTS MALAD,ENDOCRINOL & MED REPROD LAB,F-75743 PARIS 15,FRANCE
[3] HOP TROUSSEAU,EXPLORAT FONCTIONNELLES LAB,F-75571 PARIS 12,FRANCE
[4] MEM SLOAN KETTERING CANC CTR,HUMAN IMMUNOGENET LAB,NEW YORK,NY 10021
关键词
D O I
10.1007/BF00280494
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:402 / 408
页数:7
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