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No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers
被引:48
作者
:
Murray, A
论文数:
0
引用数:
0
h-index:
0
机构:
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Murray, A
[
1
]
Ennis, S
论文数:
0
引用数:
0
h-index:
0
机构:
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Ennis, S
Morton, N
论文数:
0
引用数:
0
h-index:
0
机构:
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Morton, N
机构
:
[1]
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
[2]
Southampton Univ Hosp Trust, Human Genet Res Div, Southampton, Hants, England
来源
:
AMERICAN JOURNAL OF HUMAN GENETICS
|
2000年
/ 67卷
/ 01期
关键词
:
D O I
:
10.1086/302963
中图分类号
:
Q3 [遗传学];
学科分类号
:
071007 ;
090102 ;
摘要
:
引用
收藏
页码:253 / 254
页数:2
相关论文
共 4 条
[1]
Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations
[J].
Hundscheid, RDL
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Hundscheid, RDL
;
Sistermans, EA
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Sistermans, EA
;
Thomas, CMG
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Thomas, CMG
;
Braat, DDM
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Braat, DDM
;
Straatman, H
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Straatman, H
;
Kiemeney, LALM
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Kiemeney, LALM
;
Oostra, BA
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Oostra, BA
;
Smits, APT
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Smits, APT
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2000,
66
(02)
:413
-418
[2]
POPULATION-GENETICS OF THE FRAGILE-X SYNDROME - MULTIALLELIC MODEL FOR THE FMR1 LOCUS
[J].
MORTON, NE
论文数:
0
引用数:
0
h-index:
0
机构:
SALISBURY DIST HOSP,WESSEX REG GENET LAB,SALISBURY SP2 8BJ,ENGLAND
SALISBURY DIST HOSP,WESSEX REG GENET LAB,SALISBURY SP2 8BJ,ENGLAND
MORTON, NE
;
MACPHERSON, JN
论文数:
0
引用数:
0
h-index:
0
机构:
SALISBURY DIST HOSP,WESSEX REG GENET LAB,SALISBURY SP2 8BJ,ENGLAND
SALISBURY DIST HOSP,WESSEX REG GENET LAB,SALISBURY SP2 8BJ,ENGLAND
MACPHERSON, JN
.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
1992,
89
(09)
:4215
-4217
[3]
Studies of FRAXA and FRAXE in women with premature ovarian failure
[J].
Murray, A
论文数:
0
引用数:
0
h-index:
0
机构:
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Murray, A
;
Webb, J
论文数:
0
引用数:
0
h-index:
0
机构:
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Webb, J
;
Grimley, S
论文数:
0
引用数:
0
h-index:
0
机构:
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Grimley, S
;
Conway, G
论文数:
0
引用数:
0
h-index:
0
机构:
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Conway, G
;
Jacobs, P
论文数:
0
引用数:
0
h-index:
0
机构:
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Jacobs, P
.
JOURNAL OF MEDICAL GENETICS,
1998,
35
(08)
:637
-640
[4]
MURRAY A, IN PRESS EUR J HUM G
←
1
→
共 4 条
[1]
Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations
[J].
Hundscheid, RDL
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Hundscheid, RDL
;
Sistermans, EA
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Sistermans, EA
;
Thomas, CMG
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Thomas, CMG
;
Braat, DDM
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Braat, DDM
;
Straatman, H
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Straatman, H
;
Kiemeney, LALM
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Kiemeney, LALM
;
Oostra, BA
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Oostra, BA
;
Smits, APT
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Nijmegen Hosp, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
Smits, APT
.
AMERICAN JOURNAL OF HUMAN GENETICS,
2000,
66
(02)
:413
-418
[2]
POPULATION-GENETICS OF THE FRAGILE-X SYNDROME - MULTIALLELIC MODEL FOR THE FMR1 LOCUS
[J].
MORTON, NE
论文数:
0
引用数:
0
h-index:
0
机构:
SALISBURY DIST HOSP,WESSEX REG GENET LAB,SALISBURY SP2 8BJ,ENGLAND
SALISBURY DIST HOSP,WESSEX REG GENET LAB,SALISBURY SP2 8BJ,ENGLAND
MORTON, NE
;
MACPHERSON, JN
论文数:
0
引用数:
0
h-index:
0
机构:
SALISBURY DIST HOSP,WESSEX REG GENET LAB,SALISBURY SP2 8BJ,ENGLAND
SALISBURY DIST HOSP,WESSEX REG GENET LAB,SALISBURY SP2 8BJ,ENGLAND
MACPHERSON, JN
.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
1992,
89
(09)
:4215
-4217
[3]
Studies of FRAXA and FRAXE in women with premature ovarian failure
[J].
Murray, A
论文数:
0
引用数:
0
h-index:
0
机构:
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Murray, A
;
Webb, J
论文数:
0
引用数:
0
h-index:
0
机构:
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Webb, J
;
Grimley, S
论文数:
0
引用数:
0
h-index:
0
机构:
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Grimley, S
;
Conway, G
论文数:
0
引用数:
0
h-index:
0
机构:
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Conway, G
;
Jacobs, P
论文数:
0
引用数:
0
h-index:
0
机构:
Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
Jacobs, P
.
JOURNAL OF MEDICAL GENETICS,
1998,
35
(08)
:637
-640
[4]
MURRAY A, IN PRESS EUR J HUM G
←
1
→