首页
学术期刊
论文检测
AIGC检测
热点
更多
数据
CLONING AND CHARACTERIZATION OF FIBRILLIN CDNA, A CANDIDATE GENE FOR THE MARFAN-SYNDROME
被引:0
|
作者
:
MASLEN, CL
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,PORTLAND,OR
MASLEN, CL
CORSON, GM
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,PORTLAND,OR
CORSON, GM
SAKAI, LY
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,PORTLAND,OR
SAKAI, LY
机构
:
[1]
SHRINERS HOSP CRIPPLED CHILDREN,PORTLAND,OR
[2]
OREGON HLTH SCI UNIV,PORTLAND,OR 97201
来源
:
AMERICAN JOURNAL OF HUMAN GENETICS
|
1991年
/ 49卷
/ 04期
关键词
:
D O I
:
暂无
中图分类号
:
Q3 [遗传学];
学科分类号
:
071007 ;
090102 ;
摘要
:
引用
收藏
页码:20 / 20
页数:1
相关论文
共 50 条
[1]
CLONING AND ANALYSIS OF THE CANDIDATE FIBRILLIN GENE FOR MARFAN-SYNDROME
LEE, B
论文数:
0
引用数:
0
h-index:
0
机构:
MT SINAI MED CTR,BROOKDALE CTR MOLEC BIOL,NEW YORK,NY 10029
LEE, B
VITALE, E
论文数:
0
引用数:
0
h-index:
0
机构:
MT SINAI MED CTR,BROOKDALE CTR MOLEC BIOL,NEW YORK,NY 10029
VITALE, E
RAMIREZ, F
论文数:
0
引用数:
0
h-index:
0
机构:
MT SINAI MED CTR,BROOKDALE CTR MOLEC BIOL,NEW YORK,NY 10029
RAMIREZ, F
MATTEI, MG
论文数:
0
引用数:
0
h-index:
0
机构:
MT SINAI MED CTR,BROOKDALE CTR MOLEC BIOL,NEW YORK,NY 10029
MATTEI, MG
GODFREY, M
论文数:
0
引用数:
0
h-index:
0
机构:
MT SINAI MED CTR,BROOKDALE CTR MOLEC BIOL,NEW YORK,NY 10029
GODFREY, M
HOLLISTER, D
论文数:
0
引用数:
0
h-index:
0
机构:
MT SINAI MED CTR,BROOKDALE CTR MOLEC BIOL,NEW YORK,NY 10029
HOLLISTER, D
AMERICAN JOURNAL OF HUMAN GENETICS,
1991,
49
(04)
: 20
-
20
[2]
MUTATIONS IN THE FIBRILLIN GENE AND VARIABILITY OF THE MARFAN-SYNDROME
DIETZ, HC
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, CTR MED GENET, BALTIMORE, MD 21205 USA
JOHNS HOPKINS UNIV, SCH MED, CTR MED GENET, BALTIMORE, MD 21205 USA
DIETZ, HC
PYERITZ, RE
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, CTR MED GENET, BALTIMORE, MD 21205 USA
JOHNS HOPKINS UNIV, SCH MED, CTR MED GENET, BALTIMORE, MD 21205 USA
PYERITZ, RE
CUTTING, GR
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, CTR MED GENET, BALTIMORE, MD 21205 USA
JOHNS HOPKINS UNIV, SCH MED, CTR MED GENET, BALTIMORE, MD 21205 USA
CUTTING, GR
FRANCOMANO, CA
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV, SCH MED, CTR MED GENET, BALTIMORE, MD 21205 USA
JOHNS HOPKINS UNIV, SCH MED, CTR MED GENET, BALTIMORE, MD 21205 USA
FRANCOMANO, CA
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY,
1992,
24
: S76
-
S76
[3]
THE MARFAN-SYNDROME IS CAUSED BY A POINT MUTATION IN THE FIBRILLIN GENE
MAUMENEE, IH
论文数:
0
引用数:
0
h-index:
0
机构:
Baltimore, Md
MAUMENEE, IH
ARCHIVES OF OPHTHALMOLOGY,
1992,
110
(04)
: 472
-
473
[4]
PARTIAL SEQUENCE OF A CANDIDATE GENE FOR THE MARFAN-SYNDROME
MASLEN, CL
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,3101 SW SAM JACKSON PK RD,PORTLAND,OR 97201
MASLEN, CL
CORSON, GM
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,3101 SW SAM JACKSON PK RD,PORTLAND,OR 97201
CORSON, GM
MADDOX, BK
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,3101 SW SAM JACKSON PK RD,PORTLAND,OR 97201
MADDOX, BK
GLANVILLE, RW
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,3101 SW SAM JACKSON PK RD,PORTLAND,OR 97201
GLANVILLE, RW
SAKAI, LY
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,3101 SW SAM JACKSON PK RD,PORTLAND,OR 97201
SAKAI, LY
NATURE,
1991,
352
(6333)
: 334
-
337
[5]
ABNORMAL FIBRILLIN METABOLISM IN BOVINE MARFAN-SYNDROME
POTTER, KA
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,PORTLAND,OR
POTTER, KA
HOFFMAN, Y
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,PORTLAND,OR
HOFFMAN, Y
SAKAI, LY
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,PORTLAND,OR
SAKAI, LY
BYERS, PH
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,PORTLAND,OR
BYERS, PH
BESSER, TE
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,PORTLAND,OR
BESSER, TE
MILEWICZ, DM
论文数:
0
引用数:
0
h-index:
0
机构:
SHRINERS HOSP CRIPPLED CHILDREN,PORTLAND,OR
MILEWICZ, DM
AMERICAN JOURNAL OF PATHOLOGY,
1993,
142
(03):
: 803
-
810
[6]
MARFAN-SYNDROME CAUSED BY A RECURRENT DENOVO MISSENSE MUTATION IN THE FIBRILLIN GENE
DIETZ, HC
论文数:
0
引用数:
0
h-index:
0
机构:
OREGON HLTH SCI UNIV, SHRINERS HOSP CRIPPLED CHILDREN, PORTLAND, OR 97201 USA
DIETZ, HC
CUTTING, GR
论文数:
0
引用数:
0
h-index:
0
机构:
OREGON HLTH SCI UNIV, SHRINERS HOSP CRIPPLED CHILDREN, PORTLAND, OR 97201 USA
CUTTING, GR
PYERITZ, RE
论文数:
0
引用数:
0
h-index:
0
机构:
OREGON HLTH SCI UNIV, SHRINERS HOSP CRIPPLED CHILDREN, PORTLAND, OR 97201 USA
PYERITZ, RE
MASLEN, CL
论文数:
0
引用数:
0
h-index:
0
机构:
OREGON HLTH SCI UNIV, SHRINERS HOSP CRIPPLED CHILDREN, PORTLAND, OR 97201 USA
MASLEN, CL
SAKAI, LY
论文数:
0
引用数:
0
h-index:
0
机构:
OREGON HLTH SCI UNIV, SHRINERS HOSP CRIPPLED CHILDREN, PORTLAND, OR 97201 USA
SAKAI, LY
CORSON, GM
论文数:
0
引用数:
0
h-index:
0
机构:
OREGON HLTH SCI UNIV, SHRINERS HOSP CRIPPLED CHILDREN, PORTLAND, OR 97201 USA
CORSON, GM
PUFFENBERGER, EG
论文数:
0
引用数:
0
h-index:
0
机构:
OREGON HLTH SCI UNIV, SHRINERS HOSP CRIPPLED CHILDREN, PORTLAND, OR 97201 USA
PUFFENBERGER, EG
HAMOSH, A
论文数:
0
引用数:
0
h-index:
0
机构:
OREGON HLTH SCI UNIV, SHRINERS HOSP CRIPPLED CHILDREN, PORTLAND, OR 97201 USA
HAMOSH, A
NANTHAKUMAR, EJ
论文数:
0
引用数:
0
h-index:
0
机构:
OREGON HLTH SCI UNIV, SHRINERS HOSP CRIPPLED CHILDREN, PORTLAND, OR 97201 USA
NANTHAKUMAR, EJ
CURRISTIN, SM
论文数:
0
引用数:
0
h-index:
0
机构:
OREGON HLTH SCI UNIV, SHRINERS HOSP CRIPPLED CHILDREN, PORTLAND, OR 97201 USA
CURRISTIN, SM
STETTEN, G
论文数:
0
引用数:
0
h-index:
0
机构:
OREGON HLTH SCI UNIV, SHRINERS HOSP CRIPPLED CHILDREN, PORTLAND, OR 97201 USA
STETTEN, G
MEYERS, DA
论文数:
0
引用数:
0
h-index:
0
机构:
OREGON HLTH SCI UNIV, SHRINERS HOSP CRIPPLED CHILDREN, PORTLAND, OR 97201 USA
MEYERS, DA
FRANCOMANO, CA
论文数:
0
引用数:
0
h-index:
0
机构:
OREGON HLTH SCI UNIV, SHRINERS HOSP CRIPPLED CHILDREN, PORTLAND, OR 97201 USA
FRANCOMANO, CA
NATURE,
1991,
352
(6333)
: 337
-
339
[7]
DIFFERENTIAL ALLELIC EXPRESSION OF A FIBRILLIN GENE (FBNI) IN PATIENTS WITH MARFAN-SYNDROME
HEWETT, D
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,JOHN RADCLIFFE HOSP,INST MOLEC MED,OXFORD OX3 9DU,ENGLAND
HEWETT, D
LYNCH, J
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,JOHN RADCLIFFE HOSP,INST MOLEC MED,OXFORD OX3 9DU,ENGLAND
LYNCH, J
CHILD, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,JOHN RADCLIFFE HOSP,INST MOLEC MED,OXFORD OX3 9DU,ENGLAND
CHILD, A
FIRTH, H
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,JOHN RADCLIFFE HOSP,INST MOLEC MED,OXFORD OX3 9DU,ENGLAND
FIRTH, H
SYKES, B
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,JOHN RADCLIFFE HOSP,INST MOLEC MED,OXFORD OX3 9DU,ENGLAND
SYKES, B
AMERICAN JOURNAL OF HUMAN GENETICS,
1994,
55
(03)
: 447
-
452
[8]
A NEW MISSENSE MUTATION OF FIBRILLIN IN A PATIENT WITH MARFAN-SYNDROME
HEWETT, DR
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,JOHN RADCLIFFE HOSP,INST MOLEC MED,COLLAGEN GENET GRP,OXFORD OX3 9DU,ENGLAND
HEWETT, DR
LYNCH, JR
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,JOHN RADCLIFFE HOSP,INST MOLEC MED,COLLAGEN GENET GRP,OXFORD OX3 9DU,ENGLAND
LYNCH, JR
CHILD, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,JOHN RADCLIFFE HOSP,INST MOLEC MED,COLLAGEN GENET GRP,OXFORD OX3 9DU,ENGLAND
CHILD, A
SYKES, BC
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,JOHN RADCLIFFE HOSP,INST MOLEC MED,COLLAGEN GENET GRP,OXFORD OX3 9DU,ENGLAND
SYKES, BC
JOURNAL OF MEDICAL GENETICS,
1994,
31
(04)
: 338
-
339
[9]
MUTATIONS IN THE FIBRILLIN GENE RESPONSIBLE FOR DOMINANT ECTOPIA LENTIS AND NEONATAL MARFAN-SYNDROME
KAINULAINEN, K
论文数:
0
引用数:
0
h-index:
0
机构:
NATL PUBL HLTH INST,DEPT HUMAN MOLEC GENET,SF-00300 HELSINKI,FINLAND
KAINULAINEN, K
KARTTUNEN, L
论文数:
0
引用数:
0
h-index:
0
机构:
NATL PUBL HLTH INST,DEPT HUMAN MOLEC GENET,SF-00300 HELSINKI,FINLAND
KARTTUNEN, L
PUHAKKA, L
论文数:
0
引用数:
0
h-index:
0
机构:
NATL PUBL HLTH INST,DEPT HUMAN MOLEC GENET,SF-00300 HELSINKI,FINLAND
PUHAKKA, L
SAKAI, L
论文数:
0
引用数:
0
h-index:
0
机构:
NATL PUBL HLTH INST,DEPT HUMAN MOLEC GENET,SF-00300 HELSINKI,FINLAND
SAKAI, L
PELTONEN, L
论文数:
0
引用数:
0
h-index:
0
机构:
NATL PUBL HLTH INST,DEPT HUMAN MOLEC GENET,SF-00300 HELSINKI,FINLAND
PELTONEN, L
NATURE GENETICS,
1994,
6
(01)
: 64
-
69
[10]
SCREENING OF MARFAN-SYNDROME PATIENTS FOR MUTATIONS IN THE FIBRILLIN (FBN1) GENE
论文数:
引用数:
h-index:
机构:
HAYWARD, C
LOGIE, LJ
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,WESTERN GEN HOSP,HUMAN GENET UNIT,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
UNIV EDINBURGH,WESTERN GEN HOSP,HUMAN GENET UNIT,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
LOGIE, LJ
PORTEOUS, MEM
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,WESTERN GEN HOSP,HUMAN GENET UNIT,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
UNIV EDINBURGH,WESTERN GEN HOSP,HUMAN GENET UNIT,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
PORTEOUS, MEM
BROCK, DJH
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV EDINBURGH,WESTERN GEN HOSP,HUMAN GENET UNIT,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
UNIV EDINBURGH,WESTERN GEN HOSP,HUMAN GENET UNIT,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
BROCK, DJH
JOURNAL OF MEDICAL GENETICS,
1995,
32
(02)
: 137
-
137
←
1
2
3
4
5
→