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VSX1 mutation and corneal dystrophies
被引:10
作者
:
Aldave, AJ
论文数:
0
引用数:
0
h-index:
0
Aldave, AJ
机构
:
来源
:
OPHTHALMOLOGY
|
2005年
/ 112卷
/ 01期
关键词
:
D O I
:
10.1016/j.ophtha.2004.10.017
中图分类号
:
R77 [眼科学];
学科分类号
:
100212 ;
摘要
:
引用
收藏
页码:170 / 171
页数:2
相关论文
共 3 条
[1]
ALDAVE A, IN PRESS CORNEA
[2]
VSX1:: A gene for posterior polymorphous dystrophy and keratoconus
[J].
Héon, E
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Héon, E
;
Greenberg, A
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Greenberg, A
;
Kopp, KK
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Kopp, KK
;
Rootman, D
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Rootman, D
;
Vincent, AL
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Vincent, AL
;
Billingsley, G
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Billingsley, G
;
Priston, M
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Priston, M
;
Dorval, KM
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Dorval, KM
;
Chow, RL
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Chow, RL
;
McInnes, RR
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
McInnes, RR
;
Heathcote, G
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Heathcote, G
;
Westall, C
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Westall, C
;
Sutphin, JE
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Sutphin, JE
;
Semina, E
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Semina, E
;
Bremner, R
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Bremner, R
;
Stone, EM
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Stone, EM
.
HUMAN MOLECULAR GENETICS,
2002,
11
(09)
:1029
-1036
[3]
VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells
[J].
Mintz-Hittner, HA
论文数:
0
引用数:
0
h-index:
0
机构:
Med Coll Wisconsin, Dept Pediat, Milwaukee, WI 53226 USA
Mintz-Hittner, HA
;
Semina, EV
论文数:
0
引用数:
0
h-index:
0
机构:
Med Coll Wisconsin, Dept Pediat, Milwaukee, WI 53226 USA
Semina, EV
;
Frishman, LJ
论文数:
0
引用数:
0
h-index:
0
机构:
Med Coll Wisconsin, Dept Pediat, Milwaukee, WI 53226 USA
Frishman, LJ
;
Prager, TC
论文数:
0
引用数:
0
h-index:
0
机构:
Med Coll Wisconsin, Dept Pediat, Milwaukee, WI 53226 USA
Prager, TC
;
Murray, JC
论文数:
0
引用数:
0
h-index:
0
机构:
Med Coll Wisconsin, Dept Pediat, Milwaukee, WI 53226 USA
Murray, JC
.
OPHTHALMOLOGY,
2004,
111
(04)
:828
-836
←
1
→
共 3 条
[1]
ALDAVE A, IN PRESS CORNEA
[2]
VSX1:: A gene for posterior polymorphous dystrophy and keratoconus
[J].
Héon, E
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Héon, E
;
Greenberg, A
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Greenberg, A
;
Kopp, KK
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Kopp, KK
;
Rootman, D
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Rootman, D
;
Vincent, AL
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Vincent, AL
;
Billingsley, G
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Billingsley, G
;
Priston, M
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Priston, M
;
Dorval, KM
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Dorval, KM
;
Chow, RL
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Chow, RL
;
McInnes, RR
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
McInnes, RR
;
Heathcote, G
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Heathcote, G
;
Westall, C
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Westall, C
;
Sutphin, JE
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Sutphin, JE
;
Semina, E
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Semina, E
;
Bremner, R
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Bremner, R
;
Stone, EM
论文数:
0
引用数:
0
h-index:
0
机构:
Toronto Western Res Inst, Cellular & Mol Div, Toronto, ON M5T 2S8, Canada
Stone, EM
.
HUMAN MOLECULAR GENETICS,
2002,
11
(09)
:1029
-1036
[3]
VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells
[J].
Mintz-Hittner, HA
论文数:
0
引用数:
0
h-index:
0
机构:
Med Coll Wisconsin, Dept Pediat, Milwaukee, WI 53226 USA
Mintz-Hittner, HA
;
Semina, EV
论文数:
0
引用数:
0
h-index:
0
机构:
Med Coll Wisconsin, Dept Pediat, Milwaukee, WI 53226 USA
Semina, EV
;
Frishman, LJ
论文数:
0
引用数:
0
h-index:
0
机构:
Med Coll Wisconsin, Dept Pediat, Milwaukee, WI 53226 USA
Frishman, LJ
;
Prager, TC
论文数:
0
引用数:
0
h-index:
0
机构:
Med Coll Wisconsin, Dept Pediat, Milwaukee, WI 53226 USA
Prager, TC
;
Murray, JC
论文数:
0
引用数:
0
h-index:
0
机构:
Med Coll Wisconsin, Dept Pediat, Milwaukee, WI 53226 USA
Murray, JC
.
OPHTHALMOLOGY,
2004,
111
(04)
:828
-836
←
1
→