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Mapping of a locus for a familial autosomal recessive idiopathic myoclonic epilepsy of infancy to chromosome 16p13 (vol 66, pg 1552, 2000)
被引:0
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作者
:
Zara
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0
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0
h-index:
0
Zara
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:
来源
:
AMERICAN JOURNAL OF HUMAN GENETICS
|
2000年
/ 66卷
/ 05期
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:
D O I
:
暂无
中图分类号
:
Q3 [遗传学];
学科分类号
:
071007 ;
090102 ;
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:
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页码:1728 / 1728
页数:1
相关论文
共 7 条
[1]
Mapping of a locus for a familial autosomal recessive idiopathic myoclonic epilepsy of infancy to chromosome 16p13
Zara, F
论文数:
0
引用数:
0
h-index:
0
机构:
EO Ospedali Galliera, Lab Genet Umana, I-16128 Genoa, Italy
Zara, F
Gennaro, E
论文数:
0
引用数:
0
h-index:
0
机构:
EO Ospedali Galliera, Lab Genet Umana, I-16128 Genoa, Italy
Gennaro, E
Stabile, M
论文数:
0
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0
h-index:
0
机构:
EO Ospedali Galliera, Lab Genet Umana, I-16128 Genoa, Italy
Stabile, M
Carbone, I
论文数:
0
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0
h-index:
0
机构:
EO Ospedali Galliera, Lab Genet Umana, I-16128 Genoa, Italy
Carbone, I
Malacarne, M
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0
引用数:
0
h-index:
0
机构:
EO Ospedali Galliera, Lab Genet Umana, I-16128 Genoa, Italy
Malacarne, M
Majello, L
论文数:
0
引用数:
0
h-index:
0
机构:
EO Ospedali Galliera, Lab Genet Umana, I-16128 Genoa, Italy
Majello, L
Santangelo, R
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0
引用数:
0
h-index:
0
机构:
EO Ospedali Galliera, Lab Genet Umana, I-16128 Genoa, Italy
Santangelo, R
de Falco, FA
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0
引用数:
0
h-index:
0
机构:
EO Ospedali Galliera, Lab Genet Umana, I-16128 Genoa, Italy
de Falco, FA
Bricarelli, FD
论文数:
0
引用数:
0
h-index:
0
机构:
EO Ospedali Galliera, Lab Genet Umana, I-16128 Genoa, Italy
Bricarelli, FD
AMERICAN JOURNAL OF HUMAN GENETICS,
2000,
66
(05)
: 1552
-
1557
[2]
REGIONAL MAPPING OF THE GENE FOR FAMILIAL MEDITERRANEAN FEVER ON HUMAN-CHROMOSOME 16P13
FISCHELGHODSIAN, N
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV CALIF LOS ANGELES, SCH MED, LOS ANGELES, CA USA
FISCHELGHODSIAN, N
BU, XD
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0
引用数:
0
h-index:
0
机构:
UNIV CALIF LOS ANGELES, SCH MED, LOS ANGELES, CA USA
BU, XD
PREZANT, TR
论文数:
0
引用数:
0
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0
机构:
UNIV CALIF LOS ANGELES, SCH MED, LOS ANGELES, CA USA
PREZANT, TR
OEZTAS, S
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0
引用数:
0
h-index:
0
机构:
UNIV CALIF LOS ANGELES, SCH MED, LOS ANGELES, CA USA
OEZTAS, S
HUANG, ZS
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0
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0
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0
机构:
UNIV CALIF LOS ANGELES, SCH MED, LOS ANGELES, CA USA
HUANG, ZS
BOHLMAN, MC
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0
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0
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机构:
UNIV CALIF LOS ANGELES, SCH MED, LOS ANGELES, CA USA
BOHLMAN, MC
ROTTER, JI
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0
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0
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0
机构:
UNIV CALIF LOS ANGELES, SCH MED, LOS ANGELES, CA USA
ROTTER, JI
SHOHAT, M
论文数:
0
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0
h-index:
0
机构:
UNIV CALIF LOS ANGELES, SCH MED, LOS ANGELES, CA USA
SHOHAT, M
AMERICAN JOURNAL OF MEDICAL GENETICS,
1993,
46
(06):
: 689
-
693
[3]
Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3
Finckh, U
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Hamburg, Krankenhaus Eppendorf, Inst Humangenet, D-22529 Hamburg, Germany
Finckh, U
Xu, SY
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Hamburg, Krankenhaus Eppendorf, Inst Humangenet, D-22529 Hamburg, Germany
Xu, SY
Kumaramanickavel, G
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0
引用数:
0
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0
机构:
Univ Hamburg, Krankenhaus Eppendorf, Inst Humangenet, D-22529 Hamburg, Germany
Kumaramanickavel, G
Schürmann, M
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0
引用数:
0
h-index:
0
机构:
Univ Hamburg, Krankenhaus Eppendorf, Inst Humangenet, D-22529 Hamburg, Germany
Schürmann, M
Mukkadan, JK
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0
引用数:
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机构:
Univ Hamburg, Krankenhaus Eppendorf, Inst Humangenet, D-22529 Hamburg, Germany
Mukkadan, JK
Fernandez, ST
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0
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0
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Univ Hamburg, Krankenhaus Eppendorf, Inst Humangenet, D-22529 Hamburg, Germany
Fernandez, ST
John, S
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机构:
Univ Hamburg, Krankenhaus Eppendorf, Inst Humangenet, D-22529 Hamburg, Germany
John, S
Weber, JL
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0
引用数:
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h-index:
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机构:
Univ Hamburg, Krankenhaus Eppendorf, Inst Humangenet, D-22529 Hamburg, Germany
Weber, JL
Denton, MJ
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0
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机构:
Univ Hamburg, Krankenhaus Eppendorf, Inst Humangenet, D-22529 Hamburg, Germany
Denton, MJ
Gal, A
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Univ Hamburg, Krankenhaus Eppendorf, Inst Humangenet, D-22529 Hamburg, Germany
Gal, A
GENOMICS,
1998,
48
(03)
: 341
-
345
[4]
Homozygosity mapping identifies an additional locus for Wolfram syndrome on chromosome 4q (vol 66, pg 1229, 2000)
El-Shanti, H
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El-Shanti, H
Lidral, AC
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Lidral, AC
Marazita, ML
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Marazita, ML
Cooper, ME
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Jarrah, N
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Jarrah, N
Druhan, L
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Ajlouni, K
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Ajlouni, K
AMERICAN JOURNAL OF HUMAN GENETICS,
2000,
66
(05)
: 1728
-
1728
[5]
Genetic mapping of the Camurati-Engelmann disease locus to chromosome 19q13.1q13.3 (vol 66, pg 143, 2000)
Ghadami
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AMERICAN JOURNAL OF HUMAN GENETICS,
2000,
66
(02)
: 753
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753
[6]
Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome) (vol 16, pg 88, 1997)
Matthijs, G
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0
引用数:
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Matthijs, G
NATURE GENETICS,
1997,
16
(03)
: 316
-
316
[7]
Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: Delineation of the syndrome and gene mapping to chromosome 16p12-11.2
Guerrini, R
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pisa, Inst Child Neurol & Psychiat, I-56018 Pisa, Italy
Guerrini, R
Bonanni, P
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pisa, Inst Child Neurol & Psychiat, I-56018 Pisa, Italy
Bonanni, P
Nardocci, N
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pisa, Inst Child Neurol & Psychiat, I-56018 Pisa, Italy
Nardocci, N
Parmeggiani, L
论文数:
0
引用数:
0
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0
机构:
Univ Pisa, Inst Child Neurol & Psychiat, I-56018 Pisa, Italy
Parmeggiani, L
Piccirilli, M
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0
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0
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0
机构:
Univ Pisa, Inst Child Neurol & Psychiat, I-56018 Pisa, Italy
Piccirilli, M
De Fusco, M
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0
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Univ Pisa, Inst Child Neurol & Psychiat, I-56018 Pisa, Italy
De Fusco, M
Aridon, P
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Univ Pisa, Inst Child Neurol & Psychiat, I-56018 Pisa, Italy
Aridon, P
Ballabio, A
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Ballabio, A
Carrozzo, R
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机构:
Univ Pisa, Inst Child Neurol & Psychiat, I-56018 Pisa, Italy
Carrozzo, R
Casari, G
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机构:
Univ Pisa, Inst Child Neurol & Psychiat, I-56018 Pisa, Italy
Casari, G
ANNALS OF NEUROLOGY,
1999,
45
(03)
: 344
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352
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