Physical mapping of the 5 Mb D9S196‐D9S180 interval harboring the basal cell nevus syndrome gene and localization of six genes in this region
Physical mapping of the 5 Mb D9S196‐D9S180 interval harboring the basal cell nevus syndrome gene and localization of six genes in this region
复制标题
含有基底细胞痣综合征基因的 5 Mb D9S196-D9S180 区间的物理图谱以及该区域六个基因的定位
DOI:
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发表时间:
1997
期刊:
影响因子:
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通讯作者:
E. Epstein
中科院分区:
文献类型:
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作者:
Jingwu Xie;Anthony Quinn;Xiaoli Zhang;J. Bare;Alana L. Rothman;C. Collins;S. Cutone;M. Rutter;M. K. McCormick;E. Epstein
The basal cell nevus syndrome (Gorlin syndrome) is characterized by multiple basal cell carcinomas and diverse developmental defects. The gene responsible for this syndrome has been mapped previously to a 2 cM interval between D9S196 and D9S180 at 9q22.3, and very recently mutations of a candidate gene in this region—the human homolog of the Drosophila patched gene—have been identified. We report here on physical mapping studies integrating a contig of yeast artificial chromosomes and bacterial artificial chromosomes with a long‐range map spanning approximately 5 Mb between the recombination‐determined flanking markers. Six genes have been mapped to this interval. Genes Chromosom. Cancer 18:305–309, 1997. © 1997 Wiley‐Liss, Inc.
影响因子:
4.4
作者:
D. Munroe;M. Haas;E. Bric;Tania Whitton;H. Aburatani;K. Hunter;D. Ward;D. Housman
通讯作者:
D. Munroe;M. Haas;E. Bric;Tania Whitton;H. Aburatani;K. Hunter;D. Ward;D. Housman