KRAS/NRAS/BRAF Mutation Rate in Saudi Academic Hospital Patients With Colorectal Cancer

por Saharti, Samah
Publicado 2022

The diagnostic value of add-on thyroid cell block in the evaluation of thyroid lesions

por Saharti, Samah
Publicado 2023

Next-Generation Sequencing Reveals Novel Homozygous Missense Variant c.934T > C in POLR1C Gene Causing Leukodystrophy and Hypomyelinating Disease

por Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrahman, Pushparaj, Peter Natesan, Saharti, Samah, Muthaffar, Osama Y.
Publicado 2022

Cytospin performance when using Paris system for reporting urinary cytology

por Saharti, Samah, Aljhdali, Hessa, Ajabnoor, Rana, Al Zahrani, Reem A., Daous, Yara, Refai, Fahd, Badawi, Fatima, Mokhtar, Ghadeer, Alghamdi, Doaa
Publicado 2022

The Histopathological Patterns of Ovarian Neoplasms in Different Age Groups: A Retrospective Study in a Tertiary Care Center

por Farag, Nouran H, Alsaggaf, Zahraa H, Bamardouf, Noha O, Khesfaty, Dhuha M, Fatani, Morouj M, Alghamdi, Maha K, Saharti, Samah N
Publicado 2022

Two Novel Homozygous HPS6 Mutations (Double Mutant) Identified by Whole-Exome Sequencing in a Saudi Consanguineous Family Suspected for Oculocutaneous Albinism

por Karim, Sajjad, Saharti, Samah, Alganmi, Nofe, Mirza, Zeenat, Alfares, Ahmed, Turkistany, Shereen, Al-Attas, Manal, Noureldin, Hend, Al Sakkaf, Khadega, Abusamra, Heba, Al-Qahtani, Mohammed, Abuzenadah, Adel
Publicado 2021