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Imprinting moves to the centre
被引:22
作者
:
FergusonSmith, AC
论文数:
0
引用数:
0
h-index:
0
FergusonSmith, AC
机构
:
来源
:
NATURE GENETICS
|
1996年
/ 14卷
/ 02期
关键词
:
D O I
:
10.1038/ng1096-119
中图分类号
:
Q3 [遗传学];
学科分类号
:
071007 ;
090102 ;
摘要
:
引用
收藏
页码:119 / 121
页数:3
相关论文
共 18 条
[1]
INHERITED MICRODELETIONS IN THE ANGELMAN AND PRADER-WILLI SYNDROMES DEFINE AN IMPRINTING CENTER ON HUMAN-CHROMOSOME-15
[J].
BUITING, K
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0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMAN GENET,D-45122 ESSEN,GERMANY
BUITING, K
;
SAITOH, S
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMAN GENET,D-45122 ESSEN,GERMANY
SAITOH, S
;
GROSS, S
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMAN GENET,D-45122 ESSEN,GERMANY
GROSS, S
;
DITTRICH, B
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMAN GENET,D-45122 ESSEN,GERMANY
DITTRICH, B
;
SCHWARTZ, S
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMAN GENET,D-45122 ESSEN,GERMANY
SCHWARTZ, S
;
NICHOLLS, RD
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMAN GENET,D-45122 ESSEN,GERMANY
NICHOLLS, RD
;
HORSTHEMKE, B
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMAN GENET,D-45122 ESSEN,GERMANY
HORSTHEMKE, B
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NATURE GENETICS,
1995,
9
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[2]
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
[J].
Dittrich, B
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0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMANGENET,D-45122 ESSEN,GERMANY
Dittrich, B
;
Buiting, K
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMANGENET,D-45122 ESSEN,GERMANY
Buiting, K
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Korn, B
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0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMANGENET,D-45122 ESSEN,GERMANY
Korn, B
;
Rickard, S
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMANGENET,D-45122 ESSEN,GERMANY
Rickard, S
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Buxton, J
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMANGENET,D-45122 ESSEN,GERMANY
Buxton, J
;
Saitoh, S
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMANGENET,D-45122 ESSEN,GERMANY
Saitoh, S
;
Nicholls, RD
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMANGENET,D-45122 ESSEN,GERMANY
Nicholls, RD
;
Poustka, A
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0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMANGENET,D-45122 ESSEN,GERMANY
Poustka, A
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Winterpacht, A
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0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMANGENET,D-45122 ESSEN,GERMANY
Winterpacht, A
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Zabel, B
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMANGENET,D-45122 ESSEN,GERMANY
Zabel, B
;
Horsthemke, B
论文数:
0
引用数:
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0
机构:
UNIV ESSEN GESAMTHSCH KLINIKUM,INST HUMANGENET,D-45122 ESSEN,GERMANY
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NATURE GENETICS,
1996,
14
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[3]
ELLIOT M, 1994, J MED GENET, V7, P560
[4]
EMBRYOLOGICAL AND MOLECULAR INVESTIGATIONS OF PARENTAL IMPRINTING ON MOUSE CHROMOSOME-7
[J].
FERGUSONSMITH, AC
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0
h-index:
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机构:
MRC,RADIOBIOL UNIT,OXFORD OX1 0RD,ENGLAND
MRC,RADIOBIOL UNIT,OXFORD OX1 0RD,ENGLAND
FERGUSONSMITH, AC
;
CATTANACH, BM
论文数:
0
引用数:
0
h-index:
0
机构:
MRC,RADIOBIOL UNIT,OXFORD OX1 0RD,ENGLAND
MRC,RADIOBIOL UNIT,OXFORD OX1 0RD,ENGLAND
CATTANACH, BM
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BARTON, SC
论文数:
0
引用数:
0
h-index:
0
机构:
MRC,RADIOBIOL UNIT,OXFORD OX1 0RD,ENGLAND
MRC,RADIOBIOL UNIT,OXFORD OX1 0RD,ENGLAND
BARTON, SC
;
BEECHEY, CV
论文数:
0
引用数:
0
h-index:
0
机构:
MRC,RADIOBIOL UNIT,OXFORD OX1 0RD,ENGLAND
MRC,RADIOBIOL UNIT,OXFORD OX1 0RD,ENGLAND
BEECHEY, CV
;
SURANI, MA
论文数:
0
引用数:
0
h-index:
0
机构:
MRC,RADIOBIOL UNIT,OXFORD OX1 0RD,ENGLAND
MRC,RADIOBIOL UNIT,OXFORD OX1 0RD,ENGLAND
SURANI, MA
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NATURE,
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An imprinted gene p57(KIP2) is mutated in Beckwith-Wiedemann syndrome
[J].
Hatada, I
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0
引用数:
0
h-index:
0
机构:
SAITAMA CHILDRENS MED CTR,IWATSUKI,SAITAMA 339,JAPAN
Hatada, I
;
Ohashi, H
论文数:
0
引用数:
0
h-index:
0
机构:
SAITAMA CHILDRENS MED CTR,IWATSUKI,SAITAMA 339,JAPAN
Ohashi, H
;
Fukushima, Y
论文数:
0
引用数:
0
h-index:
0
机构:
SAITAMA CHILDRENS MED CTR,IWATSUKI,SAITAMA 339,JAPAN
Fukushima, Y
;
Kaneko, Y
论文数:
0
引用数:
0
h-index:
0
机构:
SAITAMA CHILDRENS MED CTR,IWATSUKI,SAITAMA 339,JAPAN
Kaneko, Y
;
Inoue, M
论文数:
0
引用数:
0
h-index:
0
机构:
SAITAMA CHILDRENS MED CTR,IWATSUKI,SAITAMA 339,JAPAN
Inoue, M
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Komoto, Y
论文数:
0
引用数:
0
h-index:
0
机构:
SAITAMA CHILDRENS MED CTR,IWATSUKI,SAITAMA 339,JAPAN
Komoto, Y
;
Okada, A
论文数:
0
引用数:
0
h-index:
0
机构:
SAITAMA CHILDRENS MED CTR,IWATSUKI,SAITAMA 339,JAPAN
Okada, A
;
Ohishi, S
论文数:
0
引用数:
0
h-index:
0
机构:
SAITAMA CHILDRENS MED CTR,IWATSUKI,SAITAMA 339,JAPAN
Ohishi, S
;
Nabetani, A
论文数:
0
引用数:
0
h-index:
0
机构:
SAITAMA CHILDRENS MED CTR,IWATSUKI,SAITAMA 339,JAPAN
Nabetani, A
;
Morisaki, H
论文数:
0
引用数:
0
h-index:
0
机构:
SAITAMA CHILDRENS MED CTR,IWATSUKI,SAITAMA 339,JAPAN
Morisaki, H
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Nakayama, M
论文数:
0
引用数:
0
h-index:
0
机构:
SAITAMA CHILDRENS MED CTR,IWATSUKI,SAITAMA 339,JAPAN
Nakayama, M
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Niikawa, N
论文数:
0
引用数:
0
h-index:
0
机构:
SAITAMA CHILDRENS MED CTR,IWATSUKI,SAITAMA 339,JAPAN
Niikawa, N
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Mukai, T
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SAITAMA CHILDRENS MED CTR,IWATSUKI,SAITAMA 339,JAPAN
Mukai, T
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NATURE GENETICS,
1996,
14
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Genomic imprinting of human p57(KIP2) and its reduced expression in Wilms' tumors
[J].
Hatada, I
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0
引用数:
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KYOTO PREFECTURAL UNIV MED,KAMIGYO KU,KYOTO 602,JAPAN
Hatada, I
;
论文数:
引用数:
h-index:
机构:
Inazawa, J
;
Abe, T
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0
引用数:
0
h-index:
0
机构:
KYOTO PREFECTURAL UNIV MED,KAMIGYO KU,KYOTO 602,JAPAN
Abe, T
;
Nakayama, M
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO PREFECTURAL UNIV MED,KAMIGYO KU,KYOTO 602,JAPAN
Nakayama, M
;
论文数:
引用数:
h-index:
机构:
Kaneko, Y
;
Jinno, Y
论文数:
0
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0
h-index:
0
机构:
KYOTO PREFECTURAL UNIV MED,KAMIGYO KU,KYOTO 602,JAPAN
Jinno, Y
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Niikawa, N
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0
引用数:
0
h-index:
0
机构:
KYOTO PREFECTURAL UNIV MED,KAMIGYO KU,KYOTO 602,JAPAN
Niikawa, N
;
Ohashi, H
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO PREFECTURAL UNIV MED,KAMIGYO KU,KYOTO 602,JAPAN
Ohashi, H
;
Fukushima, Y
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO PREFECTURAL UNIV MED,KAMIGYO KU,KYOTO 602,JAPAN
Fukushima, Y
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Iida, K
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0
引用数:
0
h-index:
0
机构:
KYOTO PREFECTURAL UNIV MED,KAMIGYO KU,KYOTO 602,JAPAN
Iida, K
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Yutani, C
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO PREFECTURAL UNIV MED,KAMIGYO KU,KYOTO 602,JAPAN
Yutani, C
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Takahashi, S
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO PREFECTURAL UNIV MED,KAMIGYO KU,KYOTO 602,JAPAN
Takahashi, S
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Chiba, Y
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO PREFECTURAL UNIV MED,KAMIGYO KU,KYOTO 602,JAPAN
Chiba, Y
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Ohishi, S
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0
引用数:
0
h-index:
0
机构:
KYOTO PREFECTURAL UNIV MED,KAMIGYO KU,KYOTO 602,JAPAN
Ohishi, S
;
Mukai, T
论文数:
0
引用数:
0
h-index:
0
机构:
KYOTO PREFECTURAL UNIV MED,KAMIGYO KU,KYOTO 602,JAPAN
Mukai, T
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HUMAN MOLECULAR GENETICS,
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Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
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Kalikin, LM
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0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Kalikin, LM
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Johnson, LA
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0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Johnson, LA
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Alders, M
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Alders, M
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Redeker, B
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Redeker, B
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Law, DJ
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Law, DJ
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Bliek, J
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Bliek, J
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Steenman, M
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0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Steenman, M
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Benedict, M
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Benedict, M
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Wiegant, J
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0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Wiegant, J
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Lengauer, C
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0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Lengauer, C
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TaillonMiller, P
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
TaillonMiller, P
;
Schlessinger, D
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Schlessinger, D
;
Edwards, MC
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Edwards, MC
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Elledge, SJ
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0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Elledge, SJ
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Ivens, A
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Ivens, A
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Westerveld, A
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Westerveld, A
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Little, P
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0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Little, P
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Mannens, M
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0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
Mannens, M
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Feinberg, AP
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JOHNS HOPKINS UNIV, SCH MED, DEPT MED ONCOL, BALTIMORE, MD 21205 USA
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
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LAU, MMH
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STEWART, CEH
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引用数:
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h-index:
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机构:
ROCHE INST MOLEC BIOL,ROCHE RES CTR,NUTLEY,NJ 07110
STEWART, CEH
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LIU, ZY
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引用数:
0
h-index:
0
机构:
ROCHE INST MOLEC BIOL,ROCHE RES CTR,NUTLEY,NJ 07110
LIU, ZY
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BHATT, H
论文数:
0
引用数:
0
h-index:
0
机构:
ROCHE INST MOLEC BIOL,ROCHE RES CTR,NUTLEY,NJ 07110
BHATT, H
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ROTWEIN, P
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引用数:
0
h-index:
0
机构:
ROCHE INST MOLEC BIOL,ROCHE RES CTR,NUTLEY,NJ 07110
ROTWEIN, P
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STEWART, CL
论文数:
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h-index:
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机构:
UNIV GENEVA,DEPT GENET & MICROBIOL,DIV MED GENET,GENEVA,SWITZERLAND
UNIV GENEVA,DEPT GENET & MICROBIOL,DIV MED GENET,GENEVA,SWITZERLAND
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HUMAN MOLECULAR GENETICS,
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MATSUOKA, S
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EDWARDS, MC
论文数:
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引用数:
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h-index:
0
机构:
BAYLOR COLL MED,HOWARD HUGHES MED INST,HOUSTON,TX 77030
EDWARDS, MC
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BAI, C
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0
引用数:
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h-index:
0
机构:
BAYLOR COLL MED,HOWARD HUGHES MED INST,HOUSTON,TX 77030
BAI, C
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PARKER, S
论文数:
0
引用数:
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h-index:
0
机构:
BAYLOR COLL MED,HOWARD HUGHES MED INST,HOUSTON,TX 77030
PARKER, S
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ZHANG, PM
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0
引用数:
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h-index:
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机构:
BAYLOR COLL MED,HOWARD HUGHES MED INST,HOUSTON,TX 77030
ZHANG, PM
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BALDINI, A
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0
引用数:
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h-index:
0
机构:
BAYLOR COLL MED,HOWARD HUGHES MED INST,HOUSTON,TX 77030
BALDINI, A
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HARPER, JW
论文数:
0
引用数:
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h-index:
0
机构:
BAYLOR COLL MED,HOWARD HUGHES MED INST,HOUSTON,TX 77030
HARPER, JW
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ELLEDGE, SJ
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BAYLOR COLL MED,HOWARD HUGHES MED INST,HOUSTON,TX 77030
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GENES & DEVELOPMENT,
1995,
9
(06)
:650
-662
←
1
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共 18 条
[1]
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