Spectrum of germline pathogenic variants using a targeted next generation sequencing panel and genotype-phenotype correlations in patients with suspected hereditary breast cancer at an academic medical centre in Pakistan.

Autor: Akbar, Fizza1 (AUTHOR), Siddiqui, Zahraa2 (AUTHOR), Waheed, Muhammad Talha2 (AUTHOR), Ehsan, Lubaina2,3 (AUTHOR), Ali, Syed Ibaad3 (AUTHOR), Wiquar, Hajra1 (AUTHOR), Valimohammed, Azmina Tajuddin4 (AUTHOR), Khan, Shaista5 (AUTHOR), Vohra, Lubna5 (AUTHOR), Zeeshan, Sana5 (AUTHOR), Rashid, Yasmin4 (AUTHOR), Moosajee, Munira4 (AUTHOR), Jabbar, Adnan Abdul4 (AUTHOR), Zahir, Muhammad Nauman4 (AUTHOR), Zahid, Naila6 (AUTHOR), Soomro, Rufina6 (AUTHOR), Ullah, Najeeb Niamat7 (AUTHOR), Ahmad, Imran8 (AUTHOR), Haider, Ghulam9 (AUTHOR), Ansari, Uzair10 (AUTHOR)
Zdroj: Hereditary Cancer in Clinical Practice. 6/16/2022, Vol. 20 Issue 1, p1-19. 19p.
Databáze: Academic Search Ultimate
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