The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens
The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens is a paper indexed in PICO Portal from OpenAlex.
How many citations does The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens have?
The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens has 17 citations in the OpenAlex counts PICO Portal stores.
When was The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens published?
The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens has 2015 year in the PICO Portal index.
What is the open-access status of The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens?
The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens has bronze oa status in the PICO Portal index.
What is the DOI of The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens?
The DOI for The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens is on the source record.
What is the PMID of The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens?
The PMID for The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens is on the source record.
What is the OpenAlex record for The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens?
The OpenAlex for The use of FNA samples for whole‐exome sequencing and detection of somatic mutations in breast cancer surgical specimens is on the source record.