Detection of FLT3 Oncogene Mutations in Acute Myeloid Leukemia Using Conformation Sensitive Gel Electrophoresis

Por Gari, Mamdooh, Abuzenadah, Adel, Chaudhary, Adeel, Al-Qahtani, Mohammed, Banni, Huda, Ahmad, Waseem, Al-Sayes, Fatin, Lary, Sahira, Damanhouri, Ghazi
Publicado em 2008

Analysis of chromosomal and genetic disorders in patients with recurrent miscarriages in Saudi Arabia

Por Turki, Rola F, Banni, Huda A, Assidi, Mourad, Al-Qahtani, Mohammed H, Abduljabbar, Hassan S, Jamel, Hassan S, Rouzi, Abdulrahim A, Abuzenadah, Adel M
Publicado em 2014

Five novel glucose-6-phosphate dehydrogenase deficiency haplotypes correlating with disease severity

Por Dallol, Ashraf, Banni, Huda, Gari, Mamdooh A, Al-Qahtani, Mohammed H, Abuzenadeh, Adel M, Al-Sayes, Fatin, Chaudhary, Adeel G, Bidwell, Jeffrey, Kafienah, Wael
Publicado em 2012

Associations of recurrent miscarriages with chromosomal abnormalities, thrombophilia allelic polymorphisms and/or consanguinity in Saudi Arabia

Por Turki, Rola F., Assidi, Mourad, Banni, Huda A., Zahed, Hanan A., Karim, Sajjad, Schulten, Hans-Juergen, Abu-Elmagd, Muhammad, Rouzi, Abdulrahim A., Bajouh, Osama, Jamal, Hassan S., Al-Qahtani, Mohammed H., Abuzenadah, Adel M.
Publicado no BMC Med Genet (2016)

Clinical significance of frequent somatic mutations detected by high-throughput targeted sequencing in archived colorectal cancer samples

Por Dallol, Ashraf, Buhmeida, Abdelbaset, Al-Ahwal, Mahmoud Shaheen, Al-Maghrabi, Jaudah, Bajouh, Osama, Al-Khayyat, Shadi, Alam, Rania, Abusanad, Atlal, Turki, Rola, Elaimi, Aisha, Alhadrami, Hani A., Abuzenadah, Mohammed, Banni, Huda, Al-Qahtani, Mohammed H., Abuzenadah, Adel M.
Publicado no J Transl Med (2016)