10 FAMILIES WITH FRAGILE-X SYNDROME - LINKAGE RELATIONSHIPS WITH 4 DNA PROBES FROM DISTAL-XQ

被引：16

作者：

BUCHANAN, JA ^{[1
]}

BUCKTON, KE ^{[1
]}

GOSDEN, CM ^{[1
]}

NEWTON, MS ^{[1
]}

CLAYTON, JF ^{[1
]}

CHRISTIE, S ^{[1
]}

HASTIE, N ^{[1
]}

机构：

[1] WESTERN GEN HOSP,MRC,CLIN & POPULAT CYTOGENET UNIT,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND

来源：

关键词：

D O I：

10.1007/BF00284915

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：165 / 172

页数：8

共 30 条

[21] DETECTION OF SPECIFIC SEQUENCES AMONG DNA FRAGMENTS SEPARATED BY GEL-ELECTROPHORESIS
SOUTHERN, EM
[J]. JOURNAL OF MOLECULAR BIOLOGY, 1975, 98 (03) : 503 - +
[22] NEW TECHNIQUE FOR DISTINGUISHING BETWEEN HUMAN CHROMOSOMES
SUMNER, AT
EVANS, HJ
BUCKLAND, RA
[J]. NATURE-NEW BIOLOGY, 1971, 232 (27): : 31 - +
[23] CONFERENCE REPORT - 2ND INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND ON X-LINKED MENTAL-RETARDATION
TURNER, G
OPITZ, JM
BROWN, WT
DAVIES, KE
JACOBS, PA
JENKINS, EC
MIKKELSEN, M
PARTINGTON, MW
SUTHERLAND, GR
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (1-2): : 11 - 67
[24] LINKAGE AND RECOMBINATION BETWEEN FRAGILE X-LINKED MENTAL-RETARDATION AND THE FACTOR-IX GENE
WARREN, ST
GLOVER, TW
DAVIDSON, RL
JAGADEESWARAN, P
[J]. HUMAN GENETICS, 1985, 69 (01) : 44 - 46
[25] WEBB GC, 1981, LANCET, V2, P1231
[26] PRENATAL-DIAGNOSIS OF X-LINKED MENTAL-RETARDATION WITH FRAGILE (X) USING FETOSCOPY AND FETAL BLOOD-SAMPLING
WEBB, T
GOSDEN, CM
RODECK, CH
HAMILL, MA
EASON, PE
[J]. PRENATAL DIAGNOSIS, 1983, 3 (02) : 131 - 137
[27] POPULATION INCIDENCE AND SEGREGATION RATIOS IN THE MARTIN-BELL SYNDROME
WEBB, TP
BUNDEY, SE
THAKE, AI
TODD, J
[J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (1-2): : 573 - 580
[28] WINTER RM, 1986, HUM GENET, V74, P93
[29] ZOLL B, 1985, HUM GENET, V71, P122
[30] 1985, CYTOGENET CELL GENET, V40, P360