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Search Results - Aldarwish, Manar M
Search Results - Aldarwish, Manar M
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Phenotype and genotype of 15 Saudi patients with achromatopsia: A case series
by
Danish, Enam
,
Alhashem, Amal
,
Aljehani, Reham
,
Aljawi, Anan
,
Aldarwish, Manar M
,
Al Mutairi, Fuad
,
Alfadhel, Majid
,
Alrifai, Muhammad T
,
Alobaisi, Saif
Published in
Saudi journal of ophthalmology
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A child with dilated cardiomyopathy and homozygous splice site variant in FLNC gene
by
Alsubhi, Afaf
,
Aldarwish, Manar
,
Agrawal, Pankaj B.
,
Al Tala, Saeed M.
,
Eldadah, Osama
,
Alghamdi, Abdulla A.
,
Silmi, Amal
,
Almannai, Mohammed
Published in
Molecular genetics and metabolism reports
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Mutated VWA8 Is Associated With Developmental Delay, Microcephaly, and Scoliosis and Plays a Novel Role in Early Development and Skeletal Morphogenesis in Zebrafish
by
Umair, Muhammad
,
Farooq Khan, Muhammad
,
Aldrees, Mohammed
,
Nashabat, Marwan
,
Alhamoudi, Kheloud M.
,
Bilal, Muhammad
,
Alyafee, Yusra
,
Al Tuwaijri, Abeer
,
Aldarwish, Manar
,
Al-Rumayyan, Ahmed
,
Alkhalaf, Hamad
,
Wadaan, Mohammad A. M.
,
Alfadhel, Majid
Published in
Frontiers in cell and developmental biology
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A child with dilated cardiomyopathy and homozygous splice site variant in FLNC gene
by
Alsubhi, Afaf
,
Aldarwish, Manar
,
Agrawal, Pankaj B
,
Al Tala, Saeed M
,
Eldadah, Osama
,
Alghamdi, Abdulla A
,
Silmi, Amal
,
Almannai, Mohammed
Published in
Molecular genetics and metabolism reports
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Saudi Journal Of Ophthalmology
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Activating Transcription Factor 6
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Color Blindness
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Cyclic Nucleotide‐Gated Channel Subunit Alpha 3
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Inherited Retinal Diseases And Gene Therapy Update
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