LINKAGE ANALYSIS IN FRAGILE-X SYNDROME

被引：0

作者：

GRAHAM, CA ^{[1
]}

GRIER, DG ^{[1
]}

CLARKSON, M ^{[1
]}

STEWART, FJ ^{[1
]}

NEVIN, NC ^{[1
]}

机构：

[1] BELFAST CITY HOSP,CTR REG GENET,BELFAST BT9 7AB,NORTH IRELAND

来源：

CYTOGENETICS AND CELL GENETICS | 1991年 / 58卷 / 3-4期

关键词：

D O I：

暂无

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

引用

页码：2065 / 2065

页数：1

共 5 条

[1] ARVEILER B, 1988, AM J HUM GENET, V42, P380
[2] 2 ANONYMOUS X-SPECIFIC HUMAN SEQUENCES DETECTING RESTRICTION FRAGMENT LENGTH POLYMORPHISMS IN REGION XQ26-]QTER
BOGGS, BA
NUSSBAUM, RL
[J]. SOMATIC CELL AND MOLECULAR GENETICS, 1984, 10 (06) : 607 - 613
[3] BROWN TW, 1991, AM J MED GENET, V38, P343
[4] NEW POLYMORPHIC DNA MARKER CLOSE TO THE FRAGILE SITE FRAXA
OOSTRA, BA
HUPKES, PE
PERDON, LF
VANBENNEKOM, CA
BAKKER, E
HALLEY, DJJ
SCHMIDT, M
DUSART, D
SMITS, A
WIERINGA, B
VANOOST, BA
[J]. GENOMICS, 1990, 6 (01) : 129 - 132
[5] A NEW DNA MARKER TIGHTLY LINKED TO THE FRAGILE-X LOCUS (FRAXA)
SUTHERS, GK
CALLEN, DF
HYLAND, VJ
KOZMAN, HM
BAKER, E
EYRE, H
HARPER, PS
ROBERTS, SH
HORSCAYLA, MC
DAVIES, KE
BELL, MV
SUTHERLAND, GR
[J]. SCIENCE, 1989, 246 (4935) : 1298 - 1300