High-throughput genotyping of a common deletion polymorphism disrupting the TRY6 gene and its association with breast cancer risk

BACKGROUND: Copy number polymorphisms caused by genomic rearrangements like deletions, make a significant contribution to the genomic differences between two individuals and may add to disease predisposition. Therefore, genotyping of such deletion polymorphisms in case-control studies could give imp...

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Autori principali: Wagner, Kerstin, Grzybowska, Ewa, Butkiewicz, Dorota, Pamula-Pilat, Jolanta, Pekala, Wioletta, Tecza, Karolina, Hemminki, Kari, Försti, Asta
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2007
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Methodology Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1925117/
https://ncbi.nlm.nih.gov/pubmed/17598925
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-8-41
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