BRCA1基因中的减数分裂微缺失断点与对称DNA序列元件显著相关。 - Suppr

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超能文献

Meiotic microdeletion breakpoints in the BRCA1 gene are significantly associated with symmetric DNA-sequence elements.

作者信息

Schmucker B, Krawczak M

出版信息

Am J Hum Genet. 1997 Dec;61(6):1454-6. doi: 10.1086/301631.

DOI:10.1086/301631

PMID:9399889

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1716079/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fa4/1716079/976a7ec4faae/ajhg00012-0251-a.jpg

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本文引用的文献

Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancer.在10个乳腺癌/卵巢癌家族中检测到8种BRCA1突变，其中包括1个患有男性乳腺癌的家族。

Am J Hum Genet. 1995 Jul;57(1):1-7.

Chi hotspots of generalized recombination.广义重组的热点区域。

Cell. 1983 Oct;34(3):709-10. doi: 10.1016/0092-8674(83)90525-1.

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment.导致人类遗传疾病的基因缺失：诱变机制及局部DNA序列环境的作用

Hum Genet. 1991 Mar;86(5):425-41. doi: 10.1007/BF00194629.

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