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A ‘de novo’ splice site deletion in the OFD1 gene is responsible for oral–facial–digital type 1 syndrome in an Emirati child
by
Aljneibe, MA
,
Khozaimy, KM
,
Al-Kathiri, KM
,
Alameri, SS
,
Ben-Salem, S
,
Ali, BR
,
Al-Gazali, L
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Hamdan medical journal (Online)
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