Search Results - Alganmi, Nofe
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Two Novel Homozygous HPS6 Mutations (Double Mutant) Identified by Whole-Exome Sequencing in a Saudi Consanguineous Family Suspected for Oculocutaneous Albinism by 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
Published 2021Text -
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Meta-analysis of whole-genome gene expression datasets assessing the effects of IDH1 and IDH2 mutations in isogenic disease models by Schulten, Hans-Juergen, Al-Adwani, Fatima, Saddeq, Haneen A. Bin, Alkhatabi, Heba, Alganmi, Nofe, Karim, Sajjad, Hussein, Deema, Al-Ghamdi, Khalid B., Jamal, Awatif, Al-Maghrabi, Jaudah, Al-Qahtani, Mohammed H.
Published 2022Text