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Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1

While sequence analysis is considered by many to be the most sensitive method of detecting unknown mutations in large genes such as BRCA1, most published estimates of the prevalence of mutations in this gene have been derived from studies that have used other methods of gene analysis. In order to de...

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書誌詳細
主要な著者: Eng, C., Brody, L., Wagner, T., Devilee, P., Vijg, J., Szabo, C., Tavtigian, S., Nathanson, K., Ostrander, E., Frank, T.
フォーマット: Artigo
言語:Inglês
出版事項: BMJ Group 2001
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734796/
https://ncbi.nlm.nih.gov/pubmed/11748305
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.38.12.824
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