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Öğe A homozygous missense variant inTUBGCP2alter the g-tubulin ring complex leading to abnormal cortical development, pontocerebellar atrophy and altered myelination(Springernature, 2020) Oktay, Y.; Gungor, S.; Hiz, S.; Yaramis, A.; Aranguren-Ibanez, A.; Yis, U.; Sonmezler, E.[Abstract Not Available]Öğe A novel mutation in the coiled-coil interaction domain of LAMB1 extends the molecular basis of laminin-related cortical malformation phenotypes(Nature Publishing Group, 2019) Yilmaz, E.; Sonmezler, E.; Topf, A.; Balaraju, S.; Yaramis, A.; Gungor, S.; Laurie, S.[Abstract Not Available]Öğe Unexpected genetic diagnosis of mitochondrial disease in three consanguineous Turkish families(Pergamon-Elsevier Science Ltd, 2018) Topf, A.; Oktay, Y.; Balaraju, S.; Yilmaz, E.; Sonmezler, E.; Yaramis, A.; Gungor, S.[Abstract Not Available]
