Pages that link to "Q43218212"
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The following pages link to An Alu-mediated 6-kb duplication in the BRCA1 gene: a new founder mutation? (Q43218212):
Displaying 50 items.
- After BRCA1 and BRCA2-what next? Multifactorial segregation analyses of three-generation, population-based Australian families affected by female breast cancer (Q24535695) (← links)
- Characterization of a novel large deletion and single point mutations in the BRCA1 gene in a Greek cohort of families with suspected hereditary breast cancer (Q24796063) (← links)
- Nuclear function of Alus (Q28658599) (← links)
- Genome instability in blood cells of a BRCA1+ breast cancer family (Q33651926) (← links)
- Genetic testing for breast cancer predisposition (Q33779214) (← links)
- Rapid detection of novel BRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragments (Q33961119) (← links)
- Genomic rearrangements in the BRCA1 and BRCA2 genes. (Q33986463) (← links)
- Compound heterozygosity for a recurrent 16.5-kb Alu-mediated deletion mutation and single-base-pair substitutions in the ABCC6 gene results in pseudoxanthoma elasticum (Q34113251) (← links)
- Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer (Q34113283) (← links)
- The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations. The BRCA1 Exon 13 Duplication Screening Group (Q34141842) (← links)
- Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing (Q34144140) (← links)
- The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes (Q34145680) (← links)
- Morphological predictors of BRCA1 germline mutations in young women with breast cancer. (Q34727284) (← links)
- Uptake of clinical genetic testing for ovarian cancer in Ontario: a population-based study (Q34783837) (← links)
- Characterization of an Italian founder mutation in the RING-finger domain of BRCA1. (Q35091400) (← links)
- Alu elements mediate MYB gene tandem duplication in human T-ALL (Q36294397) (← links)
- BRCA1 and BRCA2 mutations in breast and ovarian cancer syndrome: reflection on the Creighton University historical series of high risk families (Q36417803) (← links)
- Evaluation of models to predict BRCA germline mutations (Q36611734) (← links)
- Screening for BRCA2 mutations in 81 Dutch breast-ovarian cancer families (Q36620818) (← links)
- BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families (Q36694756) (← links)
- Distinct BRCA1 rearrangements involving the BRCA1 pseudogene suggest the existence of a recombination hot spot (Q37216697) (← links)
- The relative contribution of point mutations and genomic rearrangements in BRCA1 and BRCA2 in high-risk breast cancer families (Q37364392) (← links)
- The contribution of BRCA1 and BRCA2 to ovarian cancer (Q37453854) (← links)
- Mutational analysis of BRCA1 and BRCA2 genes in Peruvian families with hereditary breast and ovarian cancer. (Q41696477) (← links)
- Genomic rearrangements of the BRCA1 gene in Chilean breast cancer families: an MLPA analysis (Q43569224) (← links)
- KRAB zinc finger proteins. (Q46327518) (← links)
- Prevalence of BRCA1 and BRCA2 germ line mutations among women with carcinoma of the fallopian tube (Q46366935) (← links)
- A specific GFP expression assay, penetrance estimate, and histological assessment for a putative splice site mutation in BRCA1. (Q47818883) (← links)
- Extranodal marginal zone B-cell lymphoma genotyping by Alu-polymerase chain reaction (Q47835724) (← links)
- Different molecular mechanisms underlie genomic deletions in the MLH1 Gene (Q48276381) (← links)
- Characterization of a new BRCA1 rearrangement in an Italian woman with hereditary breast and ovarian cancer syndrome (Q50645287) (← links)
- Exclusion of large deletions and other rearrangements in BRCA1 and BRCA2 in Finnish breast and ovarian cancer families. (Q52934654) (← links)
- Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriers. (Q52978695) (← links)
- Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH). (Q53493348) (← links)
- Identification of the first case of germline duplication of BRCA1 exon 13 in an Italian family. (Q54448210) (← links)
- Prevalence of BRCA1 and BRCA2 germline mutations in young breast cancer patients: a population-based study. (Q54765466) (← links)
- Assessment of individuals with BRCA1 and BRCA2 large rearrangements in high-risk breast and ovarian cancer families (Q54996542) (← links)
- An alternative approach to medical genetics based on modern evolutionary biology. Part 4: HERVs in cancer. (Q55638631) (← links)
- Meta-Analysis of gross insertions causing human genetic disease: Novel mutational mechanisms and the role of replication slippage (Q57263803) (← links)
- Familial Risks, Early-Onset Breast Cancer, and BRCA1 and BRCA2 Germline Mutations (Q57306010) (← links)
- Mutation analysis of BRCA1 and BRCA2 cancer predisposition genes in radiation hypersensitive cancer patients (Q57306016) (← links)
- The BRCA1 exon 13 duplication in the Swedish population (Q57741875) (← links)
- Contribution ofBRCA1andBRCA2mutations to inherited ovarian cancer (Q59688934) (← links)
- A 10-Mb paracentric inversion of chromosome arm 2p inactivatesMSH2 and is responsible for hereditary nonpolyposis colorectal cancer in a North-American kindred (Q62977759) (← links)
- Hierarchical mutation screening protocol for the BRCA1 gene (Q73141885) (← links)
- A sporadic breast tumor with a somatically acquired complex genomic rearrangement in BRCA1 (Q73459809) (← links)
- Color bar coding the BRCA1 gene on combed DNA: a useful strategy for detecting large gene rearrangements (Q73704833) (← links)
- A deletion/insertion mutation in the BRCA2 gene in a breast cancer family: a possible role of the Alu-polyA tail in the evolution of the deletion (Q73704837) (← links)
- An Alu-mediated 7.1 kb deletion of BRCA1 exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10 (Q73912443) (← links)
- DNA array-based method for detection of large rearrangements in the BRCA1 gene (Q78294871) (← links)