Nitrogen and boron nutrition in grafted watermelon II: Impact on nutrient accumulation in fruit rind and flesh von Gülüt, Kemal Yalçin, Duymus, Ebru, Solmaz, Ilknur, Torun, Ayfer Alkan

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Artan Dozlarda Bor Uygulamasının Antep Fıstığı (Pistacia vera L.) Çeşitlerinin Yeşil Aksam Bor Konsantrasyonu ve Diğer Besin Elementlerinin Alımı Üzerine Etkisi von Alkan Torun, Ayfer, Bozgeyik, Sadettin, Duymuş, Ebru

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Ayçiçeğinde Tuz Zararı Üzerine Bor Uygulamalarının Etkisinin Belirlenmesi von Torun, Ayfer, Duymuş, Ebru, Erdem, Halil, Tolay, İnci, Cenkseven, Şahin, Gülüt, Kemal Yalçın, Torun, Bülent

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Effects of Zn Applications on Dry Matter Yield and Mineral Nutrient Uptake of Corn and Wheat Crops in Two Different Regions of Soils with Zinc Deficiency von Ayfer Alkan Torun, Ebru Duymuş, Halil Erdem, Mustafa Bülent Torun

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Çinko Noksanlığına Sahip İki Farklı Bölge Toprağına Zn Uygulamalarının Mısır ve Buğday Bitkilerinin Kuru Madde Verimine ve Mineral Besin Elementi Alımına Etkileri von Torun, Ayfer Alkan, Duymuş, Ebru, Erdem, Halil, Torun, Mustafa Bülent

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Assessment of Pathogenic Variants in the PAH Gene and Genotype-Phenotype Correlation in Phenylketonuria Patients from Turkey von Balasar, Özgür, Kadıoğlu Yılmaz, Banu, Başdemirci, Müşerref, Koçak Eker, Hatice, Eser Çavdartepe, Büşra, Şimşek, Levent, Tunçez, Ebru, Duymuş, Fahrettin

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A Turkish consanguineous family with a novel stop-gain mutation in SPTBN2 gene leads to spinocerebellar ataxia 14 von Duymus, Fahrettin, Ozdemir, Ebru Marzioglu, Kartal, Ayse

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eP208 - A Turkish consanguineous family with a novel stop-gain mutation in SPTBN2 gene leads to spinocerebellar ataxia 14 von Duymus, Fahrettin, Ozdemir, Ebru Marzioglu, Kartal, Ayse

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A novel double hemizygous BTK mutation in a boy presenting with Pseudomonas skin abscesses von Guler, Tugba, Emiroglu, Melike, Duymus, Fahrettin, Marzioglu Ozdemir, Ebru, Artac, Hasibe

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Case report: 10q26 deletion syndrome von Esin, Deniz, Duymus, Fahrettin, Tulgar, Busra Goksel, Ozdemir, Ebru Marzioglu, Cora, Tulun, Kartal, Ayse

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eP264 - A novel homozygous PGAP2 mutation causing hyperphosphatasia with mental retardation syndrome-3 von Esin, Deniz, Duymus, Fahrettin, Tulgar, Busra Goksel, Ozdemir, Ebru Marzioglu, Cora, Tulun, Kartal, Ayse

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eP269 - In silico analysis of similar protein sequences between Sars-Cov-2 and BCG vaccine von Tulgar, Busra Goksel, Duymus, Fahrettin, Esin, Deniz, Maden, Fatma Betul, Ozdemir, Ebru Marzioglu, Kocak, Nadir

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eP266 - Case report: A novel deletion in the NLRP7 gene in the genetic etiology of recurrent hydatidiform mole pregnancy von Tulgar, Busra Goksel, Esin, Deniz, Celik, Cetin, Ozdemir, Ebru Marzioglu, Duymus, Fahrettin

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eP220 - Case report: 10q26 deletion syndrome von Esin, Deniz, Duymus, Fahrettin, Tulgar, Busra Goksel, Ozdemir, Ebru Marzioglu, Cora, Tulun, Kartal, Ayse

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Case report: A novel deletion in the NLRP7 gene in the genetic etiology of recurrent hydatidiform mole pregnancy von Tulgar, Busra Goksel, Esin, Deniz, Celik, Cetin, Ozdemir, Ebru Marzioglu, Duymus, Fahrettin

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A novel homozygous PGAP2 mutation causing hyperphosphatasia with mental retardation syndrome-3 von Esin, Deniz, Duymus, Fahrettin, Tulgar, Busra Goksel, Ozdemir, Ebru Marzioglu, Cora, Tulun, Kartal, Ayse

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In silico analysis of similar protein sequences between Sars-Cov-2 and BCG vaccine von Tulgar, Busra Goksel, Duymus, Fahrettin, Esin, Deniz, Maden, Fatma Betul, Ozdemir, Ebru Marzioglu, Kocak, Nadir

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Influence of the IDOL Gene Variants on Low-Density Lipoprotein Cholesterol Levels in Turkish Patients with Familial Hypercholesterolemia von Duymus, Fahrettin, Kocak, Nadir, Özdemir, Ebru Marzioğlu, Esin, Deniz, Körez, Muslu Kazim, Cora, Tülün

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