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Call.No
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Title
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Publishing
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Author
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ISBN
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Record.No
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1
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Dis.RF292 .T6
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A novel splice site mutation in ADGVR1 detected in Palestinian family with hearing loss by next generation sequencing/by Fida Ahmad Tomizy
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Bethlehem, [ Palestine ] : Bethlehem University , 2016
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Tomizy, Fida Ahmad
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109352
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2
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Dis.RF292 .A2
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Identification of mutations causing congenital nonsyndromic hearing loss in Hanan school for the deaf in Jenin district/by Sari Hisham Mustafa Aburas
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Bethlehem, [ Palestine ] : Bethlehem University , 2017
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Aburas, Sari Hisham Mustafa
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109353
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3
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|
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Dis.RF292 .A5
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A novel mutation in GPR98 gene detected by next generation sequencing causes hearing loss in a Palestinian family/by Abeer H. Anabtawi
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Bethlehem, [ Palestine ] : Bethlehem University , 2014
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Anabtawi, Abeer H.
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109461
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4
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Dis.RF292 .A23
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Targeted next generation sequencing identifies a novel splice site mutation in Myosin VI associated with progressive nonsyndromic hearing loss/Amal Abu Rayyan
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Bethlehem, [ Palestine ] : Bethlehem University , 2013
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Abu Rayyan, Amal
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109462
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5
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Dis.RF292 .Q3
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Linkage exclusion of FBXO10 locus as a cause of hearing impairment in selected Palestinian families with the disease/Bayan Mohammad Qabaja
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Bethlehem, [ Palestine ] : Bethlehem University , 2014
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Qabaja, Bayan Mohammad
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109463
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6
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Dis. RF292 .F3
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Identification of mutations causing congenital nonsyndromic hearing loss in 29 families in West Bank and Gaza/by Issam T. Farrah
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Bethlehem, [ Palestine ] : Bethlehem University , 2021
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Farrah, Issam T.
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112316
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