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Genetic mapping of the Camurati-Engelmann disease locus to chromosome 19q13.1q13.3 (vol 66, pg 143, 2000)
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:
Ghadami
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Ghadami
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AMERICAN JOURNAL OF HUMAN GENETICS
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2000年
/ 66卷
/ 02期
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:
Q3 [遗传学];
学科分类号
:
071007 ;
090102 ;
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页码:753 / 753
页数:1
相关论文
共 20 条
[1]
Genetic mapping of the Camurati-Engelmann disease locus to chromosome 19q13.1-q13.3
Ghadami, M
论文数:
0
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0
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0
机构:
Nagasaki Univ, Sch Med, Dept Human Genet, Nagasaki 8528523, Japan
Ghadami, M
Makita, Y
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0
引用数:
0
h-index:
0
机构:
Nagasaki Univ, Sch Med, Dept Human Genet, Nagasaki 8528523, Japan
Makita, Y
Yoshida, K
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0
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0
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0
机构:
Nagasaki Univ, Sch Med, Dept Human Genet, Nagasaki 8528523, Japan
Yoshida, K
Nishimura, G
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0
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0
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Nagasaki Univ, Sch Med, Dept Human Genet, Nagasaki 8528523, Japan
Nishimura, G
Fukushima, Y
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0
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Nagasaki Univ, Sch Med, Dept Human Genet, Nagasaki 8528523, Japan
Fukushima, Y
Wakui, K
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0
引用数:
0
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Nagasaki Univ, Sch Med, Dept Human Genet, Nagasaki 8528523, Japan
Wakui, K
Ikegawa, S
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0
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Nagasaki Univ, Sch Med, Dept Human Genet, Nagasaki 8528523, Japan
Ikegawa, S
Yamada, K
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0
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Nagasaki Univ, Sch Med, Dept Human Genet, Nagasaki 8528523, Japan
Yamada, K
Kondo, S
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0
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Nagasaki Univ, Sch Med, Dept Human Genet, Nagasaki 8528523, Japan
Kondo, S
Niikawa, N
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0
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Nagasaki Univ, Sch Med, Dept Human Genet, Nagasaki 8528523, Japan
Niikawa, N
Tomita, H
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0
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Tomita, H
AMERICAN JOURNAL OF HUMAN GENETICS,
2000,
66
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147
[2]
Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13
Janssens, K
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Univ Antwerp, Dept Med Genet, B-2610 Antwerp, Belgium
Janssens, K
Gershoni-Baruch, R
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Gershoni-Baruch, R
Van Hul, E
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JOURNAL OF MEDICAL GENETICS,
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37
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[3]
Homozygosity mapping identifies an additional locus for Wolfram syndrome on chromosome 4q (vol 66, pg 1229, 2000)
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[4]
Identification of a locus of zinc finger genes in human chromosome 19q13.1-q13.3 region by fluorescence in situ hybridization
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FINE MAPPING AND HAPLOTYPE ANALYSIS OF THE LOCUS FOR CONGENITAL NEPHROTIC SYNDROME ON CHROMOSOME 19Q13.1
MANNIKKO, M
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UNIV OULU, BIOCTR, SF-90570 OULU, FINLAND
MANNIKKO, M
KESTILA, M
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A locus for primary ciliary dyskinesia maps to chromosome 19q (vol 37, pg 241, 2000)
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EVIDENCE FOR LINKAGE OF THE CENTRAL CORE DISEASE LOCUS TO HUMAN CHROMOSOME-19Q12-13.1
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Genetic refinement and physical mapping of a biparental complete hydatidiform mole locus on chromosome 19q13.4
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Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family:: Exclusion of MAG as a candidate gene
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