MULTIPOINT LINKAGE OF 9 ANONYMOUS PROBES TO HPRT, FACTOR-IX, AND FRAGILE-X

被引：26

作者：

BROWN, WT

YE, W

GROSS, AC

CHAN, CB

DOBKIN, CS

JENKINS, EC

机构：

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1988年 / 30卷 / 1-2期

关键词：

D O I：

10.1002/ajmg.1320300157

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：551 / 566

页数：16

共 22 条

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[5] FURTHER EVIDENCE FOR GENETIC-HETEROGENEITY IN THE FRAGILE-X SYNDROME
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[6] BROWN WT, 1988, IN PRESS HUM GENET, V78
[7] CLOSE LINKAGE OF FRAGILE X MENTAL-RETARDATION SYNDROME TO HEMOPHILIA-B AND TRANSMISSION THROUGH A NORMAL-MALE
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[8] DAVIES KE, 1985, HUM GENET, V70, P249
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[10] JENKINS EC, 1986, EXP CELL BIOL, V54, P40