Reassignment of MYCL1 to human chromosome 1p34.3 by fluorescence in situ hybridization
被引:15
作者:
Speleman, F
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机构:
UNIV ANTWERP,DEPT MED GENET,B-2020 ANTWERP,BELGIUMUNIV ANTWERP,DEPT MED GENET,B-2020 ANTWERP,BELGIUM
Speleman, F
[1
]
VanCamp, G
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机构:
UNIV ANTWERP,DEPT MED GENET,B-2020 ANTWERP,BELGIUMUNIV ANTWERP,DEPT MED GENET,B-2020 ANTWERP,BELGIUM
VanCamp, G
[1
]
VanRoy, N
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h-index: 0
机构:
UNIV ANTWERP,DEPT MED GENET,B-2020 ANTWERP,BELGIUMUNIV ANTWERP,DEPT MED GENET,B-2020 ANTWERP,BELGIUM
VanRoy, N
[1
]
机构:
[1] UNIV ANTWERP,DEPT MED GENET,B-2020 ANTWERP,BELGIUM
来源:
CYTOGENETICS AND CELL GENETICS
|
1996年
/
72卷
/
2-3期
关键词:
D O I:
10.1159/000134185
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
MYCL1 has been previously mapped to 1p32. This position was in contradiction with our mapping data of Ip deletions in neuroblastoma cell lines. Using FISH on high resolution R-banded chromosomes with a YAC clone for MYCL1 we were able to reassign the gene to subband 1p34.3. This new map position is of importance for the establishment of an integrated map for chromosome 1 and the search for disease genes in this region.