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Search Results - Alzaidan, H.I.
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Mutations in known disease genes account for the majority of autosomal recessive retinal dystrophies
by
Patel, N.
,
Alkuraya, H.
,
Alzahrani, S.S.
,
Nowailaty, S.R.
,
Seidahmed, M.Z.
,
Alhemidan, A.
,
Ben‐Omran, T.
,
Ghazi, N.G.
,
Al‐Aqeel, A.
,
Al‐Owain, M.
,
Alzaidan, H.I.
,
Faqeih, E.
,
Kurdi, W.
,
Rahbeeni, Z.
,
Ibrahim, N.
,
Abdulwahab, F.
,
Hashem, M.
,
Shaheen, R.
,
Abouelhoda, M.
,
Monies, D.
,
Khan, A.O.
,
Aldahmesh, M.A.
,
Alkuraya, Fowzan S.
Published in
Clinical genetics
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Clinical Genetics
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Disease Burden
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Gene Deletion
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Gene Mapping
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Genetics & Heredity
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Hook2
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