Literature DB >> 9399889

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

B Schmucker, M Krawczak.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1997        PMID： 9399889      PMCID： PMC1716079          DOI： 10.1086/301631

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


× No keyword cloud information.
  3 in total

1.  Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment.

Authors:  M Krawczak; D N Cooper
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

Review 2.  Chi hotspots of generalized recombination.

Authors:  G R Smith
Journal:  Cell       Date:  1983-10       Impact factor: 41.582

3.  Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancer.

Authors:  J P Struewing; L C Brody; M R Erdos; R G Kase; T R Giambarresi; S A Smith; F S Collins; M A Tucker
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025
  3 in total
  2 in total

Review 1.  Human gene mutation in pathology and evolution.

Authors:  D N Cooper
Journal:  J Inherit Metab Dis       Date:  2002-05       Impact factor: 4.982

2.  Sequence features of HLA-DRB1 locus define putative basis for gene conversion and point mutations.

Authors:  Jenny von Salomé; Jyrki P Kukkonen
Journal:  BMC Genomics       Date:  2008-05-19       Impact factor: 3.969
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.