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Abdelraouf ER
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Absence of CHRDL1 and FOXC1 sequence changes in two brothers with Megalocornea-Mental Retardation Syndrome
by
Gebril OH
,
Cheong SS
,
Hardcastle AJ
,
Abdelraouf ER
,
Eid SR
,
Elsaied M
Published 2017
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