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
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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:
Genes, Chromosomes and Cancer
影响因子:
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通讯作者:
E. Epstein
E. Epstein
中科院分区:
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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

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基底细胞痣综合征(Gorlin综合征)以多发性基底细胞癌和各种发育缺陷为特征。导致这种综合征的基因此前已经被定位在D9S196和D9S180之间2 cM的9q22.3处,最近在这个区域发现了一个候选基因的突变--果蝇补丁基因的人类同源基因。我们在这里报道了物理作图研究,整合了酵母人工染色体和细菌人工染色体的重叠群,以及在重组决定的侧翼标记之间跨越大约5Mb的长距离图谱。有六个基因被定位到这个区间。基因染色体。癌症18:305-309,1997。©1997 Wiley-Liss,Inc.
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.
DOI: 10.1006/geno.1994.1100
发表时间: 1994-02
期刊: Genomics
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