Beyond the exome: utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases.

Autor: AlAbdi, Lama1,2 (AUTHOR), Shamseldin, Hanan E.2 (AUTHOR), Khouj, Ebtissal2 (AUTHOR), Helaby, Rana2 (AUTHOR), Aljamal, Bayan2 (AUTHOR), Alqahtani, Mashael2 (AUTHOR), Almulhim, Aisha1,2 (AUTHOR), Hamid, Halima1,2 (AUTHOR), Hashem, Mais O.2 (AUTHOR), Abdulwahab, Firdous2 (AUTHOR), Abouyousef, Omar2 (AUTHOR), Jaafar, Amal2 (AUTHOR), Alshidi, Tarfa2 (AUTHOR), Al-Owain, Mohammed3,4 (AUTHOR), Alhashem, Amal4,5 (AUTHOR), Al Tala, Saeed6 (AUTHOR), Khan, Arif O.7,8 (AUTHOR), Mardawi, Elham9 (AUTHOR), Alkuraya, Hisham10 (AUTHOR), Faqeih, Eissa11 (AUTHOR)
Zdroj: Genome Medicine. 12/14/2023, Vol. 15 Issue 1, p1-16. 16p.
Databáze: Academic Search Ultimate
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