首页
学术期刊
论文检测
AIGC检测
热点
更多
数据
Evaluation of the SMN and NAIP Genes in a Family: Homozygous Deletion of the SMN2 Gene in the Fetus and Outcome of the Pregnancy
被引:2
作者
:
论文数:
引用数:
h-index:
机构:
Cogulu, Ozgur
[
1
]
Durmaz, Burak
论文数:
0
引用数:
0
h-index:
0
机构:
Ege Univ, Fac Med, Dept Med Genet, TR-35100 Izmir, Turkey
Ege Univ, Fac Med, Dept Med Genet, TR-35100 Izmir, Turkey
Durmaz, Burak
[
1
]
论文数:
引用数:
h-index:
机构:
Pehlivan, Sacide
[
2
]
Alpman, Asude
论文数:
0
引用数:
0
h-index:
0
机构:
Ege Univ, Fac Med, Dept Med Genet, TR-35100 Izmir, Turkey
Ege Univ, Fac Med, Dept Med Genet, TR-35100 Izmir, Turkey
Alpman, Asude
[
1
]
Ozkinay, Ferda
论文数:
0
引用数:
0
h-index:
0
机构:
Ege Univ, Fac Med, Dept Med Genet, TR-35100 Izmir, Turkey
Ege Univ, Fac Med, Dept Med Genet, TR-35100 Izmir, Turkey
Ozkinay, Ferda
[
1
]
机构
:
[1]
Ege Univ, Fac Med, Dept Med Genet, TR-35100 Izmir, Turkey
[2]
Ege Univ, Fac Med, Dept Biol, TR-35100 Izmir, Turkey
来源
:
GENETIC TESTING AND MOLECULAR BIOMARKERS
|
2009年
/ 13卷
/ 03期
关键词
:
SPINAL MUSCULAR-ATROPHY;
D O I
:
10.1089/gtmb.2008.0139
中图分类号
:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号
:
071010 ;
081704 ;
摘要
:
[No abstract available]
引用
收藏
页码:287 / 288
页数:2
相关论文
共 7 条
[1]
Derakhshandeh-Peykar P, 2007, ANN ACAD MED SINGAP, V36, P937
[2]
Deletion analysis in Turkish patients with spinal muscular atrophy
Erdem, H
论文数:
0
引用数:
0
h-index:
0
机构:
Hacettepe Univ, Sch Med, Dept Med Biol, TR-06100 Ankara, Turkey
Hacettepe Univ, Sch Med, Dept Med Biol, TR-06100 Ankara, Turkey
Erdem, H
Pehlivan, S
论文数:
0
引用数:
0
h-index:
0
机构:
Hacettepe Univ, Sch Med, Dept Med Biol, TR-06100 Ankara, Turkey
Pehlivan, S
Topaloglu, H
论文数:
0
引用数:
0
h-index:
0
机构:
Hacettepe Univ, Sch Med, Dept Med Biol, TR-06100 Ankara, Turkey
Topaloglu, H
Özgüç, M
论文数:
0
引用数:
0
h-index:
0
机构:
Hacettepe Univ, Sch Med, Dept Med Biol, TR-06100 Ankara, Turkey
Özgüç, M
[J].
BRAIN & DEVELOPMENT,
1999,
21
(02)
: 86
-
89
[3]
IDENTIFICATION AND CHARACTERIZATION OF A SPINAL MUSCULAR ATROPHY-DETERMINING GENE
LEFEBVRE, S
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
LEFEBVRE, S
BURGLEN, L
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
BURGLEN, L
REBOULLET, S
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
REBOULLET, S
CLERMONT, O
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
CLERMONT, O
BURLET, P
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
BURLET, P
VIOLLET, L
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
VIOLLET, L
BENICHOU, B
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
BENICHOU, B
CRUAUD, C
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
CRUAUD, C
MILLASSEAU, P
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
MILLASSEAU, P
ZEVIANI, M
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
ZEVIANI, M
LEPASLIER, D
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
LEPASLIER, D
FREZAL, J
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
FREZAL, J
COHEN, D
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
COHEN, D
WEISSENBACH, J
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
WEISSENBACH, J
MUNNICH, A
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
MUNNICH, A
MELKI, J
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
MELKI, J
[J].
CELL,
1995,
80
(01)
: 155
-
165
[4]
MacLeod M J, 1999, Eur J Paediatr Neurol, V3, P65, DOI 10.1016/S1090-3798(99)80004-X
[5]
Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families
Savas, S
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Savas, S
Eraslan, S
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Eraslan, S
Kantarci, S
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Kantarci, S
Karaman, B
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Karaman, B
Acarsoz, D
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Acarsoz, D
Tükel, T
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Tükel, T
论文数:
引用数:
h-index:
机构:
Cogulu, O
Ozkinay, F
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Ozkinay, F
Basaran, S
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Basaran, S
Aydinli, K
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Aydinli, K
Yuksel-Apak, M
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Yuksel-Apak, M
Kirdar, B
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Kirdar, B
[J].
PRENATAL DIAGNOSIS,
2002,
22
(08)
: 703
-
709
[6]
Screening of deletions in SMN, NAIP and BTF2p44 genes in Turkish spinal muscular atrophy patients
Savas, S
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Savas, S
Gokgoz, N
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Gokgoz, N
Kayserili, H
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Kayserili, H
Ozkinay, F
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Ozkinay, F
Yuksel-Apak, M
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Yuksel-Apak, M
Kirdar, B
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Kirdar, B
[J].
HUMAN HEREDITY,
2000,
50
(03)
: 162
-
165
[7]
Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotype
Talbot, K
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,DEPT BIOCHEM,GENET LAB,OXFORD OX1 3QU,ENGLAND
Talbot, K
Rodrigues, NR
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,DEPT BIOCHEM,GENET LAB,OXFORD OX1 3QU,ENGLAND
Rodrigues, NR
Ignatius, J
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,DEPT BIOCHEM,GENET LAB,OXFORD OX1 3QU,ENGLAND
Ignatius, J
Muntoni, F
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,DEPT BIOCHEM,GENET LAB,OXFORD OX1 3QU,ENGLAND
Muntoni, F
Davies, KE
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,DEPT BIOCHEM,GENET LAB,OXFORD OX1 3QU,ENGLAND
Davies, KE
[J].
NEUROMUSCULAR DISORDERS,
1997,
7
(03)
: 198
-
201
←
1
→
共 7 条
[1]
Derakhshandeh-Peykar P, 2007, ANN ACAD MED SINGAP, V36, P937
[2]
Deletion analysis in Turkish patients with spinal muscular atrophy
Erdem, H
论文数:
0
引用数:
0
h-index:
0
机构:
Hacettepe Univ, Sch Med, Dept Med Biol, TR-06100 Ankara, Turkey
Hacettepe Univ, Sch Med, Dept Med Biol, TR-06100 Ankara, Turkey
Erdem, H
Pehlivan, S
论文数:
0
引用数:
0
h-index:
0
机构:
Hacettepe Univ, Sch Med, Dept Med Biol, TR-06100 Ankara, Turkey
Pehlivan, S
Topaloglu, H
论文数:
0
引用数:
0
h-index:
0
机构:
Hacettepe Univ, Sch Med, Dept Med Biol, TR-06100 Ankara, Turkey
Topaloglu, H
Özgüç, M
论文数:
0
引用数:
0
h-index:
0
机构:
Hacettepe Univ, Sch Med, Dept Med Biol, TR-06100 Ankara, Turkey
Özgüç, M
[J].
BRAIN & DEVELOPMENT,
1999,
21
(02)
: 86
-
89
[3]
IDENTIFICATION AND CHARACTERIZATION OF A SPINAL MUSCULAR ATROPHY-DETERMINING GENE
LEFEBVRE, S
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
LEFEBVRE, S
BURGLEN, L
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
BURGLEN, L
REBOULLET, S
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
REBOULLET, S
CLERMONT, O
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
CLERMONT, O
BURLET, P
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
BURLET, P
VIOLLET, L
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
VIOLLET, L
BENICHOU, B
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
BENICHOU, B
CRUAUD, C
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
CRUAUD, C
MILLASSEAU, P
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
MILLASSEAU, P
ZEVIANI, M
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
ZEVIANI, M
LEPASLIER, D
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
LEPASLIER, D
FREZAL, J
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
FREZAL, J
COHEN, D
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
COHEN, D
WEISSENBACH, J
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
WEISSENBACH, J
MUNNICH, A
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
MUNNICH, A
MELKI, J
论文数:
0
引用数:
0
h-index:
0
机构:
CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
MELKI, J
[J].
CELL,
1995,
80
(01)
: 155
-
165
[4]
MacLeod M J, 1999, Eur J Paediatr Neurol, V3, P65, DOI 10.1016/S1090-3798(99)80004-X
[5]
Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families
Savas, S
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Savas, S
Eraslan, S
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Eraslan, S
Kantarci, S
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Kantarci, S
Karaman, B
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Karaman, B
Acarsoz, D
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Acarsoz, D
Tükel, T
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Tükel, T
论文数:
引用数:
h-index:
机构:
Cogulu, O
Ozkinay, F
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Ozkinay, F
Basaran, S
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Basaran, S
Aydinli, K
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Aydinli, K
Yuksel-Apak, M
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Yuksel-Apak, M
Kirdar, B
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey
Kirdar, B
[J].
PRENATAL DIAGNOSIS,
2002,
22
(08)
: 703
-
709
[6]
Screening of deletions in SMN, NAIP and BTF2p44 genes in Turkish spinal muscular atrophy patients
Savas, S
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Savas, S
Gokgoz, N
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Gokgoz, N
Kayserili, H
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Kayserili, H
Ozkinay, F
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Ozkinay, F
Yuksel-Apak, M
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Yuksel-Apak, M
Kirdar, B
论文数:
0
引用数:
0
h-index:
0
机构:
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Bogazici Univ, Dept Chem Engn, TR-80815 Bebek, Istanbul, Turkey
Kirdar, B
[J].
HUMAN HEREDITY,
2000,
50
(03)
: 162
-
165
[7]
Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotype
Talbot, K
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,DEPT BIOCHEM,GENET LAB,OXFORD OX1 3QU,ENGLAND
Talbot, K
Rodrigues, NR
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,DEPT BIOCHEM,GENET LAB,OXFORD OX1 3QU,ENGLAND
Rodrigues, NR
Ignatius, J
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,DEPT BIOCHEM,GENET LAB,OXFORD OX1 3QU,ENGLAND
Ignatius, J
Muntoni, F
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,DEPT BIOCHEM,GENET LAB,OXFORD OX1 3QU,ENGLAND
Muntoni, F
Davies, KE
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV OXFORD,DEPT BIOCHEM,GENET LAB,OXFORD OX1 3QU,ENGLAND
Davies, KE
[J].
NEUROMUSCULAR DISORDERS,
1997,
7
(03)
: 198
-
201
←
1
→