首页
学术期刊
论文检测
AIGC检测
热点
更多
数据
GENETIC-HETEROGENEITY IN HYPERTROPHIC CARDIOMYOPATHY - EVIDENCE THAT HCM MAPS TO CHROMOSOME 2P
被引:0
|
作者
:
EPSTEIN, N
论文数:
0
引用数:
0
h-index:
0
机构:
NHLBI,BETHESDA,MD 20892
EPSTEIN, N
FANANAPAZIR, L
论文数:
0
引用数:
0
h-index:
0
机构:
NHLBI,BETHESDA,MD 20892
FANANAPAZIR, L
LIN, H
论文数:
0
引用数:
0
h-index:
0
机构:
NHLBI,BETHESDA,MD 20892
LIN, H
MARON, BJ
论文数:
0
引用数:
0
h-index:
0
机构:
NHLBI,BETHESDA,MD 20892
MARON, BJ
MULVIHILL, J
论文数:
0
引用数:
0
h-index:
0
机构:
NHLBI,BETHESDA,MD 20892
MULVIHILL, J
WHITE, R
论文数:
0
引用数:
0
h-index:
0
机构:
NHLBI,BETHESDA,MD 20892
WHITE, R
LALOUEL, JM
论文数:
0
引用数:
0
h-index:
0
机构:
NHLBI,BETHESDA,MD 20892
LALOUEL, JM
NIENHUIS, A
论文数:
0
引用数:
0
h-index:
0
机构:
NHLBI,BETHESDA,MD 20892
NIENHUIS, A
LEPPERT, M
论文数:
0
引用数:
0
h-index:
0
机构:
NHLBI,BETHESDA,MD 20892
LEPPERT, M
机构
:
[1]
NHLBI,BETHESDA,MD 20892
[2]
HOWARD HUGHES MED INST,SALT LAKE CITY,UT
来源
:
CIRCULATION
|
1990年
/ 82卷
/ 04期
关键词
:
D O I
:
暂无
中图分类号
:
R5 [内科学];
学科分类号
:
1002 ;
100201 ;
摘要
:
引用
收藏
页码:399 / 399
页数:1
相关论文
共 50 条
[31]
EVIDENCE FOR GENETIC-HETEROGENEITY IN MALIGNANT HYPERTHERMIA SUSCEPTIBILITY
LEVITT, RC
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS MED INST,DEPT MED,BALTIMORE,MD 21205
LEVITT, RC
NOURI, N
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS MED INST,DEPT MED,BALTIMORE,MD 21205
NOURI, N
JEDLICKA, AE
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS MED INST,DEPT MED,BALTIMORE,MD 21205
JEDLICKA, AE
MCKUSICK, VA
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS MED INST,DEPT MED,BALTIMORE,MD 21205
MCKUSICK, VA
MARKS, AR
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS MED INST,DEPT MED,BALTIMORE,MD 21205
MARKS, AR
SHUTACK, JG
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS MED INST,DEPT MED,BALTIMORE,MD 21205
SHUTACK, JG
FLETCHER, JE
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS MED INST,DEPT MED,BALTIMORE,MD 21205
FLETCHER, JE
ROSENBERG, H
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS MED INST,DEPT MED,BALTIMORE,MD 21205
ROSENBERG, H
MEYERS, DA
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS MED INST,DEPT MED,BALTIMORE,MD 21205
MEYERS, DA
GENOMICS,
1991,
11
(03)
: 543
-
547
[32]
ANDROGEN INSENSITIVITY IN MAN - EVIDENCE FOR GENETIC-HETEROGENEITY
AMRHEIN, JA
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,BALTIMORE,MD 21205
AMRHEIN, JA
MEYER, WJ
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,BALTIMORE,MD 21205
MEYER, WJ
JONES, HW
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,BALTIMORE,MD 21205
JONES, HW
MIGEON, CJ
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,BALTIMORE,MD 21205
MIGEON, CJ
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
1976,
73
(03)
: 891
-
894
[33]
EVIDENCE OF GENETIC-HETEROGENEITY IN THE LONG QT SYNDROME
BENHORIN, J
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,INST LIFE SCI,DEPT GENET,IL-91904 JERUSALEM,ISRAEL
BENHORIN, J
KALMAN, YM
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,INST LIFE SCI,DEPT GENET,IL-91904 JERUSALEM,ISRAEL
KALMAN, YM
MEDINA, A
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,INST LIFE SCI,DEPT GENET,IL-91904 JERUSALEM,ISRAEL
MEDINA, A
TOWBIN, J
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,INST LIFE SCI,DEPT GENET,IL-91904 JERUSALEM,ISRAEL
TOWBIN, J
RAVEHAREL, N
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,INST LIFE SCI,DEPT GENET,IL-91904 JERUSALEM,ISRAEL
RAVEHAREL, N
DYER, TD
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,INST LIFE SCI,DEPT GENET,IL-91904 JERUSALEM,ISRAEL
DYER, TD
BLANGERO, J
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,INST LIFE SCI,DEPT GENET,IL-91904 JERUSALEM,ISRAEL
BLANGERO, J
MACCLUER, JW
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,INST LIFE SCI,DEPT GENET,IL-91904 JERUSALEM,ISRAEL
MACCLUER, JW
KEREM, BS
论文数:
0
引用数:
0
h-index:
0
机构:
HEBREW UNIV JERUSALEM,INST LIFE SCI,DEPT GENET,IL-91904 JERUSALEM,ISRAEL
KEREM, BS
SCIENCE,
1993,
260
(5116)
: 1960
-
1962
[34]
EVIDENCE OF GENETIC-HETEROGENEITY AMONG THE NONDYSTROPHIC MYOTONIAS
PTACEK, LJ
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV UTAH,SCH MED,HOWARD HUGHES MED INST,SALT LAKE CITY,UT 84132
PTACEK, LJ
ZITER, FA
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV UTAH,SCH MED,HOWARD HUGHES MED INST,SALT LAKE CITY,UT 84132
ZITER, FA
ROBERTS, JW
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV UTAH,SCH MED,HOWARD HUGHES MED INST,SALT LAKE CITY,UT 84132
ROBERTS, JW
LEPPERT, MF
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV UTAH,SCH MED,HOWARD HUGHES MED INST,SALT LAKE CITY,UT 84132
LEPPERT, MF
NEUROLOGY,
1992,
42
(05)
: 1046
-
1048
[35]
HISTORICAL EVIDENCE FOR GENETIC-HETEROGENEITY OF PSEUDOXANTHOMA ELASTICUM
POPE, FM
论文数:
0
引用数:
0
h-index:
0
机构:
ST JOHNS HOSP DIS SKIN, INST DERMATOL, LONDON WC2H 7BJ, ENGLAND
ST JOHNS HOSP DIS SKIN, INST DERMATOL, LONDON WC2H 7BJ, ENGLAND
POPE, FM
BRITISH JOURNAL OF DERMATOLOGY,
1975,
92
(05)
: 493
-
509
[36]
A FAMILIAL HYPERTROPHIC CARDIOMYOPATHY LOCUS MAPS TO CHROMOSOME-15Q2
THIERFELDER, L
论文数:
0
引用数:
0
h-index:
0
机构:
BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOL,BOSTON,MA 02115
THIERFELDER, L
MACRAE, C
论文数:
0
引用数:
0
h-index:
0
机构:
BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOL,BOSTON,MA 02115
MACRAE, C
WATKINS, H
论文数:
0
引用数:
0
h-index:
0
机构:
BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOL,BOSTON,MA 02115
WATKINS, H
TOMFOHRDE, J
论文数:
0
引用数:
0
h-index:
0
机构:
BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOL,BOSTON,MA 02115
TOMFOHRDE, J
WILLIAMS, M
论文数:
0
引用数:
0
h-index:
0
机构:
BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOL,BOSTON,MA 02115
WILLIAMS, M
MCKENNA, W
论文数:
0
引用数:
0
h-index:
0
机构:
BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOL,BOSTON,MA 02115
MCKENNA, W
BOHM, K
论文数:
0
引用数:
0
h-index:
0
机构:
BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOL,BOSTON,MA 02115
BOHM, K
NOESKE, G
论文数:
0
引用数:
0
h-index:
0
机构:
BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOL,BOSTON,MA 02115
NOESKE, G
SCHLEPPER, M
论文数:
0
引用数:
0
h-index:
0
机构:
BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOL,BOSTON,MA 02115
SCHLEPPER, M
BOWCOCK, A
论文数:
0
引用数:
0
h-index:
0
机构:
BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOL,BOSTON,MA 02115
BOWCOCK, A
VOSBERG, HP
论文数:
0
引用数:
0
h-index:
0
机构:
BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOL,BOSTON,MA 02115
VOSBERG, HP
SEIDMAN, JG
论文数:
0
引用数:
0
h-index:
0
机构:
BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOL,BOSTON,MA 02115
SEIDMAN, JG
SEIDMAN, C
论文数:
0
引用数:
0
h-index:
0
机构:
BRIGHAM & WOMENS HOSP,DEPT MED,DIV CARDIOL,BOSTON,MA 02115
SEIDMAN, C
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
1993,
90
(13)
: 6270
-
6274
[37]
LINKAGE OF A HUMAN BRAIN MALFORMATION, FAMILIAL HOLOPROSENCEPHALY, TO CHROMOSOME-7 AND EVIDENCE FOR GENETIC-HETEROGENEITY
MUENKE, M
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
MUENKE, M
GURRIERI, F
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
GURRIERI, F
BAY, C
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
BAY, C
YI, DH
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
YI, DH
COLLINS, AL
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
COLLINS, AL
JOHNSON, VP
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
JOHNSON, VP
HENNEKAM, RCM
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
HENNEKAM, RCM
SCHAEFER, GB
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
SCHAEFER, GB
WEIK, LA
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
WEIK, LA
LUBINSKY, MS
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
LUBINSKY, MS
DAACKHIRSCH, S
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
DAACKHIRSCH, S
MOORE, CA
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
MOORE, CA
DOBYNS, WB
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
DOBYNS, WB
MURRAY, JC
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
MURRAY, JC
PRICE, RA
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PENN,SCH MED,DEPT GENET,PHILADELPHIA,PA 19104
PRICE, RA
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
1994,
91
(17)
: 8102
-
8106
[38]
Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16p12-p13 and evidence for genetic heterogeneity
Capon, Francesca
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Dept Paediat & Child Hlth, London WC1E 6JJ, England
UCL, Dept Paediat & Child Hlth, London WC1E 6JJ, England
Capon, Francesca
Reece, Ashley
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Dept Paediat & Child Hlth, London WC1E 6JJ, England
UCL, Dept Paediat & Child Hlth, London WC1E 6JJ, England
Reece, Ashley
Ravindrarajah, Rathi
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Dept Paediat & Child Hlth, London WC1E 6JJ, England
UCL, Dept Paediat & Child Hlth, London WC1E 6JJ, England
Ravindrarajah, Rathi
Chung, Eddie
论文数:
0
引用数:
0
h-index:
0
机构:
UCL, Dept Paediat & Child Hlth, London WC1E 6JJ, England
UCL, Dept Paediat & Child Hlth, London WC1E 6JJ, England
Chung, Eddie
AMERICAN JOURNAL OF HUMAN GENETICS,
2006,
79
(02)
: 378
-
382
[39]
Screening for genetic variation in the adrenomedullin gene in hypertrophic cardiomyopathy (HCM) and cardiovascular disease
Brink-Spalink, V
论文数:
0
引用数:
0
h-index:
0
机构:
Charite Univ Med Berlin, Inst Clin Pharmacol & Toxicol, Dept Clin Pharmacol, D-12200 Berlin, Germany
Brink-Spalink, V
Schönfelder, J
论文数:
0
引用数:
0
h-index:
0
机构:
Charite Univ Med Berlin, Inst Clin Pharmacol & Toxicol, Dept Clin Pharmacol, D-12200 Berlin, Germany
Schönfelder, J
Kurtz, S
论文数:
0
引用数:
0
h-index:
0
机构:
Charite Univ Med Berlin, Inst Clin Pharmacol & Toxicol, Dept Clin Pharmacol, D-12200 Berlin, Germany
Kurtz, S
Regitz-Zagrosek, V
论文数:
0
引用数:
0
h-index:
0
机构:
Charite Univ Med Berlin, Inst Clin Pharmacol & Toxicol, Dept Clin Pharmacol, D-12200 Berlin, Germany
Regitz-Zagrosek, V
Paul, M
论文数:
0
引用数:
0
h-index:
0
机构:
Charite Univ Med Berlin, Inst Clin Pharmacol & Toxicol, Dept Clin Pharmacol, D-12200 Berlin, Germany
Paul, M
Herrmann, SM
论文数:
0
引用数:
0
h-index:
0
机构:
Charite Univ Med Berlin, Inst Clin Pharmacol & Toxicol, Dept Clin Pharmacol, D-12200 Berlin, Germany
Herrmann, SM
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY,
2004,
369
: R155
-
R155
[40]
THE HOLT-ORAM SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY
NEWBURYECOB, RA
论文数:
0
引用数:
0
h-index:
0
机构:
CITY HOSP NOTTINGHAM,CTR MED GENET,NOTTINGHAM,ENGLAND
NEWBURYECOB, RA
TERRETT, JA
论文数:
0
引用数:
0
h-index:
0
机构:
CITY HOSP NOTTINGHAM,CTR MED GENET,NOTTINGHAM,ENGLAND
TERRETT, JA
LEANAGE, R
论文数:
0
引用数:
0
h-index:
0
机构:
CITY HOSP NOTTINGHAM,CTR MED GENET,NOTTINGHAM,ENGLAND
LEANAGE, R
BROOK, JD
论文数:
0
引用数:
0
h-index:
0
机构:
CITY HOSP NOTTINGHAM,CTR MED GENET,NOTTINGHAM,ENGLAND
BROOK, JD
YOUNG, ID
论文数:
0
引用数:
0
h-index:
0
机构:
CITY HOSP NOTTINGHAM,CTR MED GENET,NOTTINGHAM,ENGLAND
YOUNG, ID
RAEBURN, JA
论文数:
0
引用数:
0
h-index:
0
机构:
CITY HOSP NOTTINGHAM,CTR MED GENET,NOTTINGHAM,ENGLAND
RAEBURN, JA
AMERICAN JOURNAL OF HUMAN GENETICS,
1995,
57
(04)
: 540
-
540
←
1
2
3
4
5
→