共 15 条
Stop codon at arginine 586 is the prevalent nephronopthisis type 1 mutation in Italy
被引:7
作者:

Caridi, Gianluca
论文数: 0 引用数: 0
h-index: 0
机构: Ist Giannina Gaslini, Lab Pathophysiol Uremia, I-16148 Genoa, Italy

Dagnino, Monica
论文数: 0 引用数: 0
h-index: 0
机构: Ist Giannina Gaslini, Lab Pathophysiol Uremia, I-16148 Genoa, Italy

Trivelli, Antonella
论文数: 0 引用数: 0
h-index: 0
机构: Ist Giannina Gaslini, Lab Pathophysiol Uremia, I-16148 Genoa, Italy

Emma, Francesco
论文数: 0 引用数: 0
h-index: 0
机构: Ist Giannina Gaslini, Lab Pathophysiol Uremia, I-16148 Genoa, Italy

Perfumo, Francesco
论文数: 0 引用数: 0
h-index: 0
机构: Ist Giannina Gaslini, Lab Pathophysiol Uremia, I-16148 Genoa, Italy

Ghiggeri, Gian Marco
论文数: 0 引用数: 0
h-index: 0
机构: Ist Giannina Gaslini, Lab Pathophysiol Uremia, I-16148 Genoa, Italy
机构:
[1] Ist Giannina Gaslini, Lab Pathophysiol Uremia, I-16148 Genoa, Italy
[2] Ist Giannina Gaslini, Renal Sect, I-16148 Genoa, Italy
[3] Bambino Gesu Pediat Hosp, Nephrol Sect, Rome, Italy
关键词:
nephronophthisis;
mutation analysis;
D O I:
10.1093/ndt/gfl277
中图分类号:
R3 [基础医学];
R4 [临床医学];
学科分类号:
1001 ;
1002 ;
100602 ;
摘要:
[No abstract available]
引用
收藏
页码:2301 / 2303
页数:3
相关论文
共 15 条
[1]
Children with ocular motor apraxia type Cogan carry deletions in the gene (NPHP1) for juvenile nephronophthisis
[J].
Betz, R
;
Rensing, C
;
Otto, E
;
Mincheva, A
;
Zehnder, D
;
Lichter, P
;
Hildebrandt, F
.
JOURNAL OF PEDIATRICS,
2000, 136 (06)
:828-831

Betz, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Univ Childrens Hosp, D-79106 Freiburg, Germany

Rensing, C
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Univ Childrens Hosp, D-79106 Freiburg, Germany

Otto, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Univ Childrens Hosp, D-79106 Freiburg, Germany

Mincheva, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Univ Childrens Hosp, D-79106 Freiburg, Germany

Zehnder, D
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Univ Childrens Hosp, D-79106 Freiburg, Germany

Lichter, P
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Univ Childrens Hosp, D-79106 Freiburg, Germany

Hildebrandt, F
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Univ Childrens Hosp, D-79106 Freiburg, Germany
[2]
Clinical and molecular heterogeneity of juvenile nephronophthisis in Italy: Insights from molecular screening
[J].
Caridi, G
;
Dagnino, M
;
Gusmano, R
;
Ginevri, F
;
Murer, L
;
Ghio, L
;
Piaggio, G
;
Ciardi, MR
;
Perfumo, F
;
Ghiggeri, GM
.
AMERICAN JOURNAL OF KIDNEY DISEASES,
2000, 35 (01)
:44-51

Caridi, G
论文数: 0 引用数: 0
h-index: 0
机构: G Gaslini Inst, Lab & Dept Nephrol, Genoa, Italy

Dagnino, M
论文数: 0 引用数: 0
h-index: 0
机构: G Gaslini Inst, Lab & Dept Nephrol, Genoa, Italy

Gusmano, R
论文数: 0 引用数: 0
h-index: 0
机构: G Gaslini Inst, Lab & Dept Nephrol, Genoa, Italy

Ginevri, F
论文数: 0 引用数: 0
h-index: 0
机构: G Gaslini Inst, Lab & Dept Nephrol, Genoa, Italy

Murer, L
论文数: 0 引用数: 0
h-index: 0
机构: G Gaslini Inst, Lab & Dept Nephrol, Genoa, Italy

Ghio, L
论文数: 0 引用数: 0
h-index: 0
机构: G Gaslini Inst, Lab & Dept Nephrol, Genoa, Italy

Piaggio, G
论文数: 0 引用数: 0
h-index: 0
机构: G Gaslini Inst, Lab & Dept Nephrol, Genoa, Italy

Ciardi, MR
论文数: 0 引用数: 0
h-index: 0
机构: G Gaslini Inst, Lab & Dept Nephrol, Genoa, Italy

Perfumo, F
论文数: 0 引用数: 0
h-index: 0
机构: G Gaslini Inst, Lab & Dept Nephrol, Genoa, Italy

Ghiggeri, GM
论文数: 0 引用数: 0
h-index: 0
机构: G Gaslini Inst, Lab & Dept Nephrol, Genoa, Italy
[3]
Improved strategy for molecular genetic diagnostics in juvenile nephronophthisis
[J].
Heninger, E
;
Otto, E
;
Imm, A
;
Caridi, G
;
Hildebrandt, F
.
AMERICAN JOURNAL OF KIDNEY DISEASES,
2001, 37 (06)
:1131-1139

Heninger, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany

Otto, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany

Imm, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany

Caridi, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany

Hildebrandt, F
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany
[4]
A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1
[J].
Hildebrandt, F
;
Otto, E
;
Rensing, C
;
Nothwang, HG
;
Vollmer, M
;
Adolphs, J
;
Hanusch, H
;
Brandis, M
.
NATURE GENETICS,
1997, 17 (02)
:149-153

Hildebrandt, F
论文数: 0 引用数: 0
h-index: 0
机构:
MAX PLANCK INST MOL GENET, BERLIN, GERMANY MAX PLANCK INST MOL GENET, BERLIN, GERMANY

Otto, E
论文数: 0 引用数: 0
h-index: 0
机构:
MAX PLANCK INST MOL GENET, BERLIN, GERMANY MAX PLANCK INST MOL GENET, BERLIN, GERMANY

Rensing, C
论文数: 0 引用数: 0
h-index: 0
机构:
MAX PLANCK INST MOL GENET, BERLIN, GERMANY MAX PLANCK INST MOL GENET, BERLIN, GERMANY

Nothwang, HG
论文数: 0 引用数: 0
h-index: 0
机构:
MAX PLANCK INST MOL GENET, BERLIN, GERMANY MAX PLANCK INST MOL GENET, BERLIN, GERMANY

Vollmer, M
论文数: 0 引用数: 0
h-index: 0
机构:
MAX PLANCK INST MOL GENET, BERLIN, GERMANY MAX PLANCK INST MOL GENET, BERLIN, GERMANY

Adolphs, J
论文数: 0 引用数: 0
h-index: 0
机构:
MAX PLANCK INST MOL GENET, BERLIN, GERMANY MAX PLANCK INST MOL GENET, BERLIN, GERMANY

Hanusch, H
论文数: 0 引用数: 0
h-index: 0
机构:
MAX PLANCK INST MOL GENET, BERLIN, GERMANY MAX PLANCK INST MOL GENET, BERLIN, GERMANY

Brandis, M
论文数: 0 引用数: 0
h-index: 0
机构:
MAX PLANCK INST MOL GENET, BERLIN, GERMANY MAX PLANCK INST MOL GENET, BERLIN, GERMANY
[5]
Establishing an algorithm for molecular genetic diagnostics in 127 families with juvenile nephronophthisis
[J].
Hildebrandt, F
;
Rensing, C
;
Betz, RC
;
Sommer, U
;
Birnbaum, S
;
Imm, A
;
Omran, H
;
Leipoldt, M
;
Otto, E
.
KIDNEY INTERNATIONAL,
2001, 59 (02)
:434-445

Hildebrandt, F
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany

Rensing, C
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany

Betz, RC
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany

Sommer, U
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany

Birnbaum, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany

Imm, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany

Omran, H
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany

Leipoldt, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany

Otto, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Freiburg, Childrens Hosp, D-79106 Freiburg, Germany
[6]
Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisis
[J].
Konrad, M
;
Saunier, S
;
Heidet, L
;
Silbermann, F
;
Benessy, F
;
Calado, J
;
LePaslier, D
;
Broyer, M
;
Gubler, MC
;
Antignac, C
.
HUMAN MOLECULAR GENETICS,
1996, 5 (03)
:367-371

Konrad, M
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INSERM U423,F-75743 PARIS 15,FRANCE

论文数: 引用数:
h-index:
机构:

论文数: 引用数:
h-index:
机构:

Silbermann, F
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INSERM U423,F-75743 PARIS 15,FRANCE

Benessy, F
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INSERM U423,F-75743 PARIS 15,FRANCE

Calado, J
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INSERM U423,F-75743 PARIS 15,FRANCE

LePaslier, D
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INSERM U423,F-75743 PARIS 15,FRANCE

Broyer, M
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INSERM U423,F-75743 PARIS 15,FRANCE

Gubler, MC
论文数: 0 引用数: 0
h-index: 0
机构: HOP NECKER ENFANTS MALAD,INSERM U423,F-75743 PARIS 15,FRANCE

论文数: 引用数:
h-index:
机构:
[7]
The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin
[J].
Mollet, G
;
Salomon, R
;
Gribouval, O
;
Silbermann, F
;
Bacq, D
;
Landthaler, G
;
Milford, D
;
Nayir, A
;
Rizzoni, G
;
Antignac, C
;
Saunier, S
.
NATURE GENETICS,
2002, 32 (02)
:300-305

Mollet, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, Hop Necker Enfants Malad, INSERM, U423, Paris, France

Salomon, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, Hop Necker Enfants Malad, INSERM, U423, Paris, France

Gribouval, O
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, Hop Necker Enfants Malad, INSERM, U423, Paris, France

Silbermann, F
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, Hop Necker Enfants Malad, INSERM, U423, Paris, France

Bacq, D
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, Hop Necker Enfants Malad, INSERM, U423, Paris, France

Landthaler, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, Hop Necker Enfants Malad, INSERM, U423, Paris, France

Milford, D
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, Hop Necker Enfants Malad, INSERM, U423, Paris, France

Nayir, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, Hop Necker Enfants Malad, INSERM, U423, Paris, France

Rizzoni, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, Hop Necker Enfants Malad, INSERM, U423, Paris, France

Antignac, C
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, Hop Necker Enfants Malad, INSERM, U423, Paris, France

Saunier, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Paris 05, Hop Necker Enfants Malad, INSERM, U423, Paris, France
[8]
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis
[J].
Olbrich, H
;
Fliegauf, M
;
Hoefele, J
;
Kispert, A
;
Otto, E
;
Volz, A
;
Wolf, MT
;
Sasmaz, G
;
Trauer, U
;
Reinhardt, R
;
Sudbrak, R
;
Antignac, C
;
Gretz, N
;
Walz, G
;
Schermer, B
;
Benzing, T
;
Hildebrandt, F
;
Omran, H
.
NATURE GENETICS,
2003, 34 (04)
:455-459

Olbrich, H
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

Fliegauf, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

论文数: 引用数:
h-index:
机构:

Kispert, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

Otto, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

Volz, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

Wolf, MT
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

Sasmaz, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

Trauer, U
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

Reinhardt, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

Sudbrak, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

论文数: 引用数:
h-index:
机构:

Gretz, N
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

Walz, G
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

Schermer, B
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

Benzing, T
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

Hildebrandt, F
论文数: 0 引用数: 0
h-index: 0
机构: Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany

Omran, H
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany Univ Hosp Freiburg, Dept Pediat & Adolescent Med, D-79106 Freiburg, Germany
[9]
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin
[J].
Otto, EA
;
Loeys, B
;
Khanna, H
;
Hellemans, J
;
Sudbrak, R
;
Fan, SL
;
Muerb, U
;
O'Toole, JF
;
Helou, J
;
Attanasio, M
;
Utsch, B
;
Sayer, JA
;
Lillo, C
;
Jimeno, D
;
Coucke, P
;
De Paepe, A
;
Reinhardt, R
;
Klages, S
;
Tsuda, M
;
Kawakami, I
;
Kusakabe, T
;
Omran, H
;
Imm, A
;
Tippens, M
;
Raymond, PA
;
Hill, J
;
Beales, P
;
He, S
;
Kispert, A
;
Margolis, B
;
Williams, DS
;
Swaroop, A
;
Hildebrandt, F
.
NATURE GENETICS,
2005, 37 (03)
:282-288

Otto, EA
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Loeys, B
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Khanna, H
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Hellemans, J
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Sudbrak, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Fan, SL
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Muerb, U
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

O'Toole, JF
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Helou, J
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Attanasio, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Utsch, B
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Sayer, JA
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Lillo, C
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Jimeno, D
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Coucke, P
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

De Paepe, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Reinhardt, R
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Klages, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Tsuda, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Kawakami, I
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Kusakabe, T
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Omran, H
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Imm, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Tippens, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Raymond, PA
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Hill, J
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Beales, P
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

He, S
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Kispert, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Margolis, B
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Williams, DS
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机构: Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA

Swaroop, A
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Hildebrandt, F
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Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA Univ Michigan, Dept Pediat, Ann Arbor, MI 48109 USA
[10]
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
[J].
Otto, EA
;
Schermer, B
;
Obara, T
;
O'Toole, JF
;
Hiller, KS
;
Mueller, AM
;
Ruf, RG
;
Hoefele, J
;
Beekmann, F
;
Landau, D
;
Foreman, JW
;
Goodship, JA
;
Strachan, T
;
Kispert, A
;
Wolf, MT
;
Gagnadoux, MF
;
Nivet, H
;
Antignac, C
;
Walz, G
;
Drummond, IA
;
Benzing, T
;
Hildebrandt, F
.
NATURE GENETICS,
2003, 34 (04)
:413-420

Otto, EA
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Schermer, B
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Obara, T
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O'Toole, JF
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Hiller, KS
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Mueller, AM
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Ruf, RG
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Hoefele, J
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Beekmann, F
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Landau, D
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Foreman, JW
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Goodship, JA
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Strachan, T
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Kispert, A
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Wolf, MT
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Gagnadoux, MF
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Nivet, H
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Antignac, C
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Walz, G
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Drummond, IA
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Benzing, T
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Hildebrandt, F
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