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A third locus for dominant optic atrophy on chromosome 22q
被引:56
作者
:
Barbet, F
论文数:
0
引用数:
0
h-index:
0
机构:
Hop Necker Enfants Malad, Unite Rech Handicaps Genet Enfant, F-75743 Paris 15, France
Barbet, F
Hakiki, S
论文数:
0
引用数:
0
h-index:
0
机构:
Hop Necker Enfants Malad, Unite Rech Handicaps Genet Enfant, F-75743 Paris 15, France
Hakiki, S
Orssaud, C
论文数:
0
引用数:
0
h-index:
0
机构:
Hop Necker Enfants Malad, Unite Rech Handicaps Genet Enfant, F-75743 Paris 15, France
Orssaud, C
Gerber, S
论文数:
0
引用数:
0
h-index:
0
机构:
Hop Necker Enfants Malad, Unite Rech Handicaps Genet Enfant, F-75743 Paris 15, France
Gerber, S
Perrault, I
论文数:
0
引用数:
0
h-index:
0
机构:
Hop Necker Enfants Malad, Unite Rech Handicaps Genet Enfant, F-75743 Paris 15, France
Perrault, I
Hanein, S
论文数:
0
引用数:
0
h-index:
0
机构:
Hop Necker Enfants Malad, Unite Rech Handicaps Genet Enfant, F-75743 Paris 15, France
Hanein, S
Ducroq, D
论文数:
0
引用数:
0
h-index:
0
机构:
Hop Necker Enfants Malad, Unite Rech Handicaps Genet Enfant, F-75743 Paris 15, France
Ducroq, D
Dufier, JL
论文数:
0
引用数:
0
h-index:
0
机构:
Hop Necker Enfants Malad, Unite Rech Handicaps Genet Enfant, F-75743 Paris 15, France
Dufier, JL
Munnich, A
论文数:
0
引用数:
0
h-index:
0
机构:
Hop Necker Enfants Malad, Unite Rech Handicaps Genet Enfant, F-75743 Paris 15, France
Munnich, A
Kaplan, J
论文数:
0
引用数:
0
h-index:
0
机构:
Hop Necker Enfants Malad, Unite Rech Handicaps Genet Enfant, F-75743 Paris 15, France
Kaplan, J
Rozet, JM
论文数:
0
引用数:
0
h-index:
0
机构:
Hop Necker Enfants Malad, Unite Rech Handicaps Genet Enfant, F-75743 Paris 15, France
Rozet, JM
机构
:
[1]
Hop Necker Enfants Malad, Unite Rech Handicaps Genet Enfant, F-75743 Paris 15, France
[2]
Hop Necker Enfants Malad, Serv Ophtalmol, Paris, France
来源
:
JOURNAL OF MEDICAL GENETICS
|
2005年
/ 42卷
/ 01期
关键词
:
D O I
:
10.1136/jmg.2004.025502
中图分类号
:
Q3 [遗传学];
学科分类号
:
071007 ;
090102 ;
摘要
:
引用
收藏
页数:4
相关论文
共 14 条
[1]
A comprehensive genetic map of the human genome based on 5,264 microsatellites
Dib, C
论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Dib, C
Faure, S
论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Faure, S
Fizames, C
论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Fizames, C
Samson, D
论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Samson, D
Drouot, N
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0
引用数:
0
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机构:
GENETHON SA,F-91000 EVRY,FRANCE
Drouot, N
Vignal, A
论文数:
0
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0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Vignal, A
Millasseau, P
论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Millasseau, P
Marc, S
论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Marc, S
Hazan, J
论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Hazan, J
Seboun, E
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0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Seboun, E
Lathrop, M
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0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Lathrop, M
Gyapay, G
论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Gyapay, G
Morissette, J
论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Morissette, J
Weissenbach, J
论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Weissenbach, J
[J].
NATURE,
1996,
380
(6570)
: 152
-
154
[2]
Processing of Mgm1 by the rhomboid-type protease Pcp1 is required for maintenance of mitochondrial morphology and of mitochondrial DNA
Herlan, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Munich, Adolf Butenandt Inst Physiol Chem, D-81377 Munich, Germany
Herlan, M
Vogel, F
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Munich, Adolf Butenandt Inst Physiol Chem, D-81377 Munich, Germany
Vogel, F
Bornhövd, C
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Munich, Adolf Butenandt Inst Physiol Chem, D-81377 Munich, Germany
Bornhövd, C
Neupert, W
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Munich, Adolf Butenandt Inst Physiol Chem, D-81377 Munich, Germany
Neupert, W
Reichert, AS
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Munich, Adolf Butenandt Inst Physiol Chem, D-81377 Munich, Germany
Reichert, AS
[J].
JOURNAL OF BIOLOGICAL CHEMISTRY,
2003,
278
(30)
: 27781
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27788
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CLINICOPATHOLOGIC STUDY OF AUTOSOMAL DOMINANT OPTIC ATROPHY
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0
引用数:
0
h-index:
0
机构:
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
JOHNSTON, PB
GASTER, RN
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
GASTER, RN
SMITH, VC
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
SMITH, VC
TRIPATHI, RC
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
TRIPATHI, RC
[J].
AMERICAN JOURNAL OF OPHTHALMOLOGY,
1979,
88
(05)
: 868
-
875
[4]
Kerrison JB, 1999, ARCH OPHTHALMOL-CHIC, V117, P805
[5]
Kjer B, 1996, ACTA OPHTHALMOL SCAN, V74, P3
[6]
HOMOZYGOSITY MAPPING - A WAY TO MAP HUMAN RECESSIVE TRAITS WITH THE DNA OF INBRED CHILDREN
LANDER, ES
论文数:
0
引用数:
0
h-index:
0
机构:
HARVARD UNIV,CAMBRIDGE,MA 02138
LANDER, ES
BOTSTEIN, D
论文数:
0
引用数:
0
h-index:
0
机构:
HARVARD UNIV,CAMBRIDGE,MA 02138
BOTSTEIN, D
[J].
SCIENCE,
1987,
236
(4808)
: 1567
-
1570
[7]
LATHROP GM, 1984, AM J HUM GENET, V36, P460
[8]
Lyle WM., 1990, GENETIC RISKS
[9]
Molecular and biochemical characterization of a novel oxysterol-binding protein (OSBP2) highly expressed in retina
Moreira, EF
论文数:
0
引用数:
0
h-index:
0
机构:
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
Moreira, EF
Jaworski, C
论文数:
0
引用数:
0
h-index:
0
机构:
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
Jaworski, C
Li, A
论文数:
0
引用数:
0
h-index:
0
机构:
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
Li, A
Rodriguez, IR
论文数:
0
引用数:
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h-index:
0
机构:
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
Rodriguez, IR
[J].
JOURNAL OF BIOLOGICAL CHEMISTRY,
2001,
276
(21)
: 18570
-
18578
[10]
Linkage studies in dominant optic atrophy, Kjer type: possible evidence for heterogeneity
Seller, MJ
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Guys Hosp, Div Med & Mol Genet, London SE1 9RT, England
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Burdon, MA
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0
引用数:
0
h-index:
0
机构:
Guys Hosp, Div Med & Mol Genet, London SE1 9RT, England
Spalton, DJ
[J].
JOURNAL OF MEDICAL GENETICS,
1997,
34
(12)
: 967
-
972
←
1
2
→
共 14 条
[1]
A comprehensive genetic map of the human genome based on 5,264 microsatellites
Dib, C
论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Dib, C
Faure, S
论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Faure, S
Fizames, C
论文数:
0
引用数:
0
h-index:
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机构:
GENETHON SA,F-91000 EVRY,FRANCE
Fizames, C
Samson, D
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0
引用数:
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h-index:
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机构:
GENETHON SA,F-91000 EVRY,FRANCE
Samson, D
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论文数:
0
引用数:
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h-index:
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GENETHON SA,F-91000 EVRY,FRANCE
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论文数:
0
引用数:
0
h-index:
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机构:
GENETHON SA,F-91000 EVRY,FRANCE
Vignal, A
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0
引用数:
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h-index:
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机构:
GENETHON SA,F-91000 EVRY,FRANCE
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h-index:
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引用数:
0
h-index:
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论文数:
0
引用数:
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h-index:
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机构:
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论文数:
0
引用数:
0
h-index:
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论文数:
0
引用数:
0
h-index:
0
机构:
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论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Morissette, J
Weissenbach, J
论文数:
0
引用数:
0
h-index:
0
机构:
GENETHON SA,F-91000 EVRY,FRANCE
Weissenbach, J
[J].
NATURE,
1996,
380
(6570)
: 152
-
154
[2]
Processing of Mgm1 by the rhomboid-type protease Pcp1 is required for maintenance of mitochondrial morphology and of mitochondrial DNA
Herlan, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Munich, Adolf Butenandt Inst Physiol Chem, D-81377 Munich, Germany
Herlan, M
Vogel, F
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Munich, Adolf Butenandt Inst Physiol Chem, D-81377 Munich, Germany
Vogel, F
Bornhövd, C
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Munich, Adolf Butenandt Inst Physiol Chem, D-81377 Munich, Germany
Bornhövd, C
Neupert, W
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Munich, Adolf Butenandt Inst Physiol Chem, D-81377 Munich, Germany
Neupert, W
Reichert, AS
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Munich, Adolf Butenandt Inst Physiol Chem, D-81377 Munich, Germany
Reichert, AS
[J].
JOURNAL OF BIOLOGICAL CHEMISTRY,
2003,
278
(30)
: 27781
-
27788
[3]
CLINICOPATHOLOGIC STUDY OF AUTOSOMAL DOMINANT OPTIC ATROPHY
JOHNSTON, PB
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
JOHNSTON, PB
GASTER, RN
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
GASTER, RN
SMITH, VC
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
SMITH, VC
TRIPATHI, RC
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
UNIV CHICAGO, DEPT OPHTHALMOL, CHICAGO, IL 60637 USA
TRIPATHI, RC
[J].
AMERICAN JOURNAL OF OPHTHALMOLOGY,
1979,
88
(05)
: 868
-
875
[4]
Kerrison JB, 1999, ARCH OPHTHALMOL-CHIC, V117, P805
[5]
Kjer B, 1996, ACTA OPHTHALMOL SCAN, V74, P3
[6]
HOMOZYGOSITY MAPPING - A WAY TO MAP HUMAN RECESSIVE TRAITS WITH THE DNA OF INBRED CHILDREN
LANDER, ES
论文数:
0
引用数:
0
h-index:
0
机构:
HARVARD UNIV,CAMBRIDGE,MA 02138
LANDER, ES
BOTSTEIN, D
论文数:
0
引用数:
0
h-index:
0
机构:
HARVARD UNIV,CAMBRIDGE,MA 02138
BOTSTEIN, D
[J].
SCIENCE,
1987,
236
(4808)
: 1567
-
1570
[7]
LATHROP GM, 1984, AM J HUM GENET, V36, P460
[8]
Lyle WM., 1990, GENETIC RISKS
[9]
Molecular and biochemical characterization of a novel oxysterol-binding protein (OSBP2) highly expressed in retina
Moreira, EF
论文数:
0
引用数:
0
h-index:
0
机构:
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
Moreira, EF
Jaworski, C
论文数:
0
引用数:
0
h-index:
0
机构:
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
Jaworski, C
Li, A
论文数:
0
引用数:
0
h-index:
0
机构:
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
Li, A
Rodriguez, IR
论文数:
0
引用数:
0
h-index:
0
机构:
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
NEI, NIH, Retinal Cell & Mol Biol Lab, Bethesda, MD 20892 USA
Rodriguez, IR
[J].
JOURNAL OF BIOLOGICAL CHEMISTRY,
2001,
276
(21)
: 18570
-
18578
[10]
Linkage studies in dominant optic atrophy, Kjer type: possible evidence for heterogeneity
Seller, MJ
论文数:
0
引用数:
0
h-index:
0
机构:
Guys Hosp, Div Med & Mol Genet, London SE1 9RT, England
Seller, MJ
Behnam, JT
论文数:
0
引用数:
0
h-index:
0
机构:
Guys Hosp, Div Med & Mol Genet, London SE1 9RT, England
Behnam, JT
Lewis, CM
论文数:
0
引用数:
0
h-index:
0
机构:
Guys Hosp, Div Med & Mol Genet, London SE1 9RT, England
Lewis, CM
Johnston, RL
论文数:
0
引用数:
0
h-index:
0
机构:
Guys Hosp, Div Med & Mol Genet, London SE1 9RT, England
Johnston, RL
Burdon, MA
论文数:
0
引用数:
0
h-index:
0
机构:
Guys Hosp, Div Med & Mol Genet, London SE1 9RT, England
Burdon, MA
Spalton, DJ
论文数:
0
引用数:
0
h-index:
0
机构:
Guys Hosp, Div Med & Mol Genet, London SE1 9RT, England
Spalton, DJ
[J].
JOURNAL OF MEDICAL GENETICS,
1997,
34
(12)
: 967
-
972
←
1
2
→