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El-Bassyouni, Hala T
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Showing results 1 to 4 of 4
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Issue Date
Title
Author(s)
2013
Clinical and molecular findings in eight Egyptian patients with suspected mitochondrial disorders and optic atrophy
Al-Ettribi, Ghada MM; Effat, Laila K; El-Bassyouni, Hala T; Zaki, Maha S; Shanab, Gamila
; Karim, Amr
2014
Screening for common mutations in four FANCA gene exons in Egyptian Fanconi anemia patients
El-Bassyouni, Hala T; El-Kamah, Ghada Y; Zarouk, Waheba A; Eid, Maha M; Mosaad, Rehab M; Temtamy, Samia A; Ahmed Sayed
; Salem, Ahmed M
2013
Screening seven common mitochondrial mutations in 28 Egyptian patients with suspected mitochondrial disease
Al-Ettribi, Ghada MM; Effat, Laila K; El-Bassyouni, Hala T; Zaki, Maha S; Shanab, Gamila
; Karim, Amr M
2013
Screening seven common mitochondrial mutations in 28 Egyptian patients with suspected mitochondrial disease
Al-Ettribi, Ghada MM; Effat, Laila K; El-Bassyouni, Hala T; Zaki, Maha S; Shanab, Gamila; Karim, Amr
