Variable expressivity of patched mutations in flies and humans.
作者信息
Bale A E
出版信息
Am J Hum Genet. 1997 Jan;60(1):10-2.
Abstract
摘要
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本文引用的文献
1
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Nat Genet. 1996 Sep;14(1):78-81. doi: 10.1038/ng0996-78.
2
Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients.两名戈林综合征患者9号染色体长臂缺失的分子分析。
Am J Hum Genet. 1996 Aug;59(2):417-22.
3
Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome.痣样基底细胞癌综合征中果蝇patched人类同源物的突变
Cell. 1996 Jun 14;85(6):841-51. doi: 10.1016/s0092-8674(00)81268-4.
4
Gene linked to commonest cancer.
Science. 1996 Jun 14;272(5268):1583-4. doi: 10.1126/science.272.5268.1583.
5
A two-hit model for developmental defects in Gorlin syndrome.戈林综合征发育缺陷的双打击模型。
Nat Genet. 1996 Jan;12(1):85-7. doi: 10.1038/ng0196-85.
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Two-hit model for sporadic congenital anomalies in mice with the disorganization mutation.具有紊乱突变的小鼠散发性先天性异常的双打击模型。
Am J Hum Genet. 1993 May;52(5):866-74.
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Mutation hotspots due to sunlight in the p53 gene of nonmelanoma skin cancers.非黑素瘤皮肤癌p53基因中由阳光导致的突变热点。
Proc Natl Acad Sci U S A. 1993 May 1;90(9):4216-20. doi: 10.1073/pnas.90.9.4216.
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Clinical findings in two African-American families with the nevoid basal cell carcinoma syndrome (NBCC).两个患有痣样基底细胞癌综合征（NBCC）的非裔美国家庭的临床发现。
Am J Med Genet. 1994 Apr 15;50(3):272-81. doi: 10.1002/ajmg.1320500311.
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