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Case report: Diagnosis of a patient with Sifrim–Hitz–Weiss syndrome, development and epileptic encephalopathy-14, and medium chain acyl-CoA dehydrogenase deficiency by Naim Zeka, Naim Zeka, Eris Zeka, Esra Zhubi, Esra Zhubi, Ilir Hoxha, Ilir Hoxha, Ilir Hoxha
Published 2023-09-01
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A new variant of MYCN gene as a cause of Feingold syndrome by Naim Zeka, Ramush Bejiqi, Abdurrahim Gerguri, Leonore Zogaj, Haki Jashari
Published 2022-05-01
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