FRAGILE-X FOUNDER EFFECT

被引：36

作者：

CHAKRAVARTI, A

机构：

[1] Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA

来源：

NATURE GENETICS | 1992年 / 1卷 / 04期

关键词：

D O I：

10.1038/ng0792-237

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：237 / 238

页数：2

共 9 条

[1] VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX
FU, YH
KUHL, DPA
PIZZUTI, A
PIERETTI, M
SUTCLIFFE, JS
RICHARDS, S
VERKERK, AJMH
HOLDEN, JJA
FENWICK, RG
WARREN, ST
OOSTRA, BA
NELSON, DL
CASKEY, CT
[J]. CELL, 1991, 67 (06) : 1047 - 1058
[2] The rate of spontaneous mutation of a human gene
Haldane, JBS
[J]. JOURNAL OF GENETICS, 1935, 31 (03) : 317 - 326
[3] IDENTIFICATION OF THE CYSTIC-FIBROSIS GENE - GENETIC-ANALYSIS
KEREM, BS
ROMMENS, JM
BUCHANAN, JA
MARKIEWICZ, D
COX, TK
CHAKRAVARTI, A
BUCHWALD, M
TSUI, LC
[J]. SCIENCE, 1989, 245 (4922) : 1073 - 1080
[4] MAPPING OF DNA INSTABILITY AT THE FRAGILE-X TO A TRINUCLEOTIDE REPEAT SEQUENCE P(CCG)N
KREMER, EJ
PRITCHARD, M
LYNCH, M
YU, S
HOLMAN, K
BAKER, E
WARREN, ST
SCHLESSINGER, D
SUTHERLAND, GR
RICHARDS, RI
[J]. SCIENCE, 1991, 252 (5013) : 1711 - 1714
[5] POPULATION-GENETICS OF THE FRAGILE-X SYNDROME - MULTIALLELIC MODEL FOR THE FMR1 LOCUS
MORTON, NE
MACPHERSON, JN
[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (09) : 4215 - 4217
[6] EVIDENCE OF FOUNDER CHROMOSOMES IN FRAGILE-X SYNDROME
RICHARDS, RI
HOLMAN, K
FRIEND, K
KREMER, E
HILLEN, D
STAPLES, A
BROWN, WT
GOONEWARDENA, P
TARLETON, J
SCHWARTZ, C
SUTHERLAND, GR
[J]. NATURE GENETICS, 1992, 1 (04) : 257 - 260
[7] FURTHER SEGREGATION ANALYSIS OF THE FRAGILE-X SYNDROME WITH SPECIAL REFERENCE TO TRANSMITTING MALES
SHERMAN, SL
JACOBS, PA
MORTON, NE
FROSTERISKENIUS, U
HOWARDPEEBLES, PN
NIELSEN, KB
PARTINGTON, MW
SUTHERLAND, GR
TURNER, G
WATSON, M
[J]. HUMAN GENETICS, 1985, 69 (04) : 289 - 299
[8] IDENTIFICATION OF A GENE (FMR-1) CONTAINING A CGG REPEAT COINCIDENT WITH A BREAKPOINT CLUSTER REGION EXHIBITING LENGTH VARIATION IN FRAGILE-X SYNDROME
VERKERK, AJMH
PIERETTI, M
SUTCLIFFE, JS
FU, YH
KUHL, DPA
PIZZUTI, A
REINER, O
RICHARDS, S
VICTORIA, MF
ZHANG, FP
EUSSEN, BE
VANOMMEN, GJB
BLONDEN, LAJ
RIGGINS, GJ
CHASTAIN, JL
KUNST, CB
GALJAARD, H
CASKEY, CT
NELSON, DL
OOSTRA, BA
WARREN, ST
[J]. CELL, 1991, 65 (05) : 905 - 914
[9] FRAGILE-X GENOTYPE CHARACTERIZED BY AN UNSTABLE REGION OF DNA
YU, S
PRITCHARD, M
KREMER, E
LYNCH, M
NANCARROW, J
BAKER, E
HOLMAN, K
MULLEY, JC
WARREN, ST
SCHLESSINGER, D
SUTHERLAND, GR
RICHARDS, RI
[J]. SCIENCE, 1991, 252 (5009) : 1179 - 1181

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