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Chromosomal aberrations, subtelomeric defects, and mental retardation
被引:12
作者
:
Baralle, D
论文数:
0
引用数:
0
h-index:
0
机构:
Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 5AQ, England
Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 5AQ, England
Baralle, D
[
1
]
机构
:
[1]
Addenbrookes Hosp, Dept Med Genet, Cambridge CB2 5AQ, England
来源
:
LANCET
|
2001年
/ 358卷
/ 9275期
关键词
:
D O I
:
10.1016/S0140-6736(00)05300-9
中图分类号
:
R5 [内科学];
学科分类号
:
1002 ;
100201 ;
摘要
:
引用
收藏
页码:7 / 8
页数:2
相关论文
共 13 条
[1]
BACking up the promises
[J].
Antonarakis, SE
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Geneva, Sch Med, Div Med Genet, CH-1211 Geneva, Switzerland
Univ Geneva, Sch Med, Div Med Genet, CH-1211 Geneva, Switzerland
Antonarakis, SE
.
NATURE GENETICS,
2001,
27
(03)
:230
-+
[2]
Genes responsible for nonspecific mental retardation
[J].
Castellví-Bel, S
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Clin & Prov, Serv Genet, Barcelona, Spain
Castellví-Bel, S
;
Milà, M
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Clin & Prov, Serv Genet, Barcelona, Spain
Milà, M
.
MOLECULAR GENETICS AND METABOLISM,
2001,
72
(02)
:104
-108
[3]
Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype?
[J].
De Vries, BBA
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Dept Clin & Mol Genet, London, England
De Vries, BBA
;
Knight, SJL
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Dept Clin & Mol Genet, London, England
Knight, SJL
;
Homfray, T
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Dept Clin & Mol Genet, London, England
Homfray, T
;
Smithson, SF
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Dept Clin & Mol Genet, London, England
Smithson, SF
;
Flint, J
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Dept Clin & Mol Genet, London, England
Flint, J
;
Winter, RM
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Dept Clin & Mol Genet, London, England
Winter, RM
.
JOURNAL OF MEDICAL GENETICS,
2001,
38
(03)
:175
-178
[4]
Clinical studies on submicroscopic subtelomeric rearrangements: a checklist
[J].
de Vries, BBA
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
de Vries, BBA
;
White, SM
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
White, SM
;
Knight, SJL
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Knight, SJL
;
Regan, R
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Regan, R
;
Homfray, T
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Homfray, T
;
Young, ID
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Young, ID
;
Super, M
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Super, M
;
McKeown, C
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
McKeown, C
;
Splitt, M
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Splitt, M
;
Quarrell, OWJ
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Quarrell, OWJ
;
Trainer, AH
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Trainer, AH
;
Niermeijer, MF
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Niermeijer, MF
;
Malcolm, S
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Malcolm, S
;
Flint, J
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Flint, J
;
Hurst, JA
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Hurst, JA
;
Winter, RM
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Winter, RM
.
JOURNAL OF MEDICAL GENETICS,
2001,
38
(03)
:145
-150
[5]
Cryptic terminal rearrangement of chromosome 22q13.32 detected by FISH in two unrelated patients
[J].
Doheny, KF
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, BALTIMORE, MD 21205 USA
Doheny, KF
;
McDermid, HE
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, BALTIMORE, MD 21205 USA
McDermid, HE
;
Harum, K
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, BALTIMORE, MD 21205 USA
Harum, K
;
Thomas, GH
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, BALTIMORE, MD 21205 USA
Thomas, GH
;
Raymond, GV
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, BALTIMORE, MD 21205 USA
Raymond, GV
.
JOURNAL OF MEDICAL GENETICS,
1997,
34
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Defining the chromosomal basis of mental handicap
[J].
Hamerton, JL
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Manitoba, Fac Med, Dept Biochem & Mol Genet, Winnipeg, MB R3E 0W3, Canada
Univ Manitoba, Fac Med, Dept Biochem & Mol Genet, Winnipeg, MB R3E 0W3, Canada
Hamerton, JL
;
Stranc, L
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Manitoba, Fac Med, Dept Biochem & Mol Genet, Winnipeg, MB R3E 0W3, Canada
Univ Manitoba, Fac Med, Dept Biochem & Mol Genet, Winnipeg, MB R3E 0W3, Canada
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LANCET,
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Subtle chromosomal rearrangements in children with unexplained mental retardation
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Knight, SJL
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0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Mol Hematol Unit, Oxford OX3 9DS, England
Knight, SJL
;
Regan, R
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Mol Hematol Unit, Oxford OX3 9DS, England
Regan, R
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Nicod, A
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Mol Hematol Unit, Oxford OX3 9DS, England
Nicod, A
;
Horsley, SW
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Mol Hematol Unit, Oxford OX3 9DS, England
Horsley, SW
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Kearney, L
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Mol Hematol Unit, Oxford OX3 9DS, England
Kearney, L
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Homfray, T
论文数:
0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Mol Hematol Unit, Oxford OX3 9DS, England
Homfray, T
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Winter, RM
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0
引用数:
0
h-index:
0
机构:
John Radcliffe Hosp, Inst Mol Med, Mol Hematol Unit, Oxford OX3 9DS, England
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引用数:
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机构:
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Flint, J
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John Radcliffe Hosp, Inst Mol Med, Mol Hematol Unit, Oxford OX3 9DS, England
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Roschke, A
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NIH,DIAGNOST DEV BRANCH,NATL CTR HUMAN GENOME RES,BETHESDA,MD 20892
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引用数:
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h-index:
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NIH,DIAGNOST DEV BRANCH,NATL CTR HUMAN GENOME RES,BETHESDA,MD 20892
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Riethman, H
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引用数:
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h-index:
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NIH,DIAGNOST DEV BRANCH,NATL CTR HUMAN GENOME RES,BETHESDA,MD 20892
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NIH,DIAGNOST DEV BRANCH,NATL CTR HUMAN GENOME RES,BETHESDA,MD 20892
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Flint, J
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引用数:
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NIH,DIAGNOST DEV BRANCH,NATL CTR HUMAN GENOME RES,BETHESDA,MD 20892
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NIH,DIAGNOST DEV BRANCH,NATL CTR HUMAN GENOME RES,BETHESDA,MD 20892
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NIH,DIAGNOST DEV BRANCH,NATL CTR HUMAN GENOME RES,BETHESDA,MD 20892
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NIH,DIAGNOST DEV BRANCH,NATL CTR HUMAN GENOME RES,BETHESDA,MD 20892
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UNIV PAVIA,DIPARTIMENTO GENET & MICROBIOL A BUZZATI TRAVERSO,I-27100 PAVIA,ITALY
SACCONE, S
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DESARIO, A
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0
引用数:
0
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机构:
UNIV PAVIA,DIPARTIMENTO GENET & MICROBIOL A BUZZATI TRAVERSO,I-27100 PAVIA,ITALY
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DELLAVALLE, G
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0
引用数:
0
h-index:
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UNIV PAVIA,DIPARTIMENTO GENET & MICROBIOL A BUZZATI TRAVERSO,I-27100 PAVIA,ITALY
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BERNARDI, G
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0
引用数:
0
h-index:
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UNIV PAVIA,DIPARTIMENTO GENET & MICROBIOL A BUZZATI TRAVERSO,I-27100 PAVIA,ITALY
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2
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共 13 条
[1]
BACking up the promises
[J].
Antonarakis, SE
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Geneva, Sch Med, Div Med Genet, CH-1211 Geneva, Switzerland
Univ Geneva, Sch Med, Div Med Genet, CH-1211 Geneva, Switzerland
Antonarakis, SE
.
NATURE GENETICS,
2001,
27
(03)
:230
-+
[2]
Genes responsible for nonspecific mental retardation
[J].
Castellví-Bel, S
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Clin & Prov, Serv Genet, Barcelona, Spain
Castellví-Bel, S
;
Milà, M
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Clin & Prov, Serv Genet, Barcelona, Spain
Milà, M
.
MOLECULAR GENETICS AND METABOLISM,
2001,
72
(02)
:104
-108
[3]
Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype?
[J].
De Vries, BBA
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Dept Clin & Mol Genet, London, England
De Vries, BBA
;
Knight, SJL
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Dept Clin & Mol Genet, London, England
Knight, SJL
;
Homfray, T
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Dept Clin & Mol Genet, London, England
Homfray, T
;
Smithson, SF
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Dept Clin & Mol Genet, London, England
Smithson, SF
;
Flint, J
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Dept Clin & Mol Genet, London, England
Flint, J
;
Winter, RM
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Dept Clin & Mol Genet, London, England
Winter, RM
.
JOURNAL OF MEDICAL GENETICS,
2001,
38
(03)
:175
-178
[4]
Clinical studies on submicroscopic subtelomeric rearrangements: a checklist
[J].
de Vries, BBA
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
de Vries, BBA
;
White, SM
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
White, SM
;
Knight, SJL
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Knight, SJL
;
Regan, R
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Regan, R
;
Homfray, T
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Homfray, T
;
Young, ID
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Young, ID
;
Super, M
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Super, M
;
McKeown, C
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
McKeown, C
;
Splitt, M
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Splitt, M
;
Quarrell, OWJ
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Quarrell, OWJ
;
Trainer, AH
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Trainer, AH
;
Niermeijer, MF
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Niermeijer, MF
;
Malcolm, S
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Malcolm, S
;
Flint, J
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Flint, J
;
Hurst, JA
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Hurst, JA
;
Winter, RM
论文数:
0
引用数:
0
h-index:
0
机构:
Inst Child Hlth, Clin & Mol Genet Unit, London WC1N 1EH, England
Winter, RM
.
JOURNAL OF MEDICAL GENETICS,
2001,
38
(03)
:145
-150
[5]
Cryptic terminal rearrangement of chromosome 22q13.32 detected by FISH in two unrelated patients
[J].
Doheny, KF
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, BALTIMORE, MD 21205 USA
Doheny, KF
;
McDermid, HE
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, BALTIMORE, MD 21205 USA
McDermid, HE
;
Harum, K
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, BALTIMORE, MD 21205 USA
Harum, K
;
Thomas, GH
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, BALTIMORE, MD 21205 USA
Thomas, GH
;
Raymond, GV
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT PEDIAT, BALTIMORE, MD 21205 USA
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JOURNAL OF MEDICAL GENETICS,
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34
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Defining the chromosomal basis of mental handicap
[J].
Hamerton, JL
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0
引用数:
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h-index:
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