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	1.	A Case-Control Association Study of [electronic resource] by Sahin-Calapoglu, Nilufer Demirci, Serpil Calapoglu, Mustafa Yasar, Baris Publication details: Parkinson's disease 2016 In: Parkinson's disease vol. 2016 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genetic study of demyelinating form of autosomal-recessive Charcot-Marie-tooth diseases in a Turkish family. [electronic resource] by Sahin-Calapoglu, Nilufer Soyoz, Mustafa Calapoglu, Mustafa Ozcelik, Nurten Producer: 20100126 In: The International journal of neuroscience vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Novel GDAP1 mutation in a Turkish family with CMT2K (CMT2K with novel GDAP1 mutation). [electronic resource] by Sahin-Calapoglu, Nilufer Tan, Meliha Soyoz, Mustafa Calapoglu, Mustafa Ozcelik, Nurten Producer: 20091005 In: Neuromolecular medicine vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Novel human pathological mutations. Gene symbol: GDAP1. Disease: Charcot-Marie-Tooth disease 4A. [electronic resource] by Sahin-Calapoglu, Nilufer Soyoz, Mustafa Tan, Meliha Calapoglu, Mustafa Ozcelik, Nurten Producer: 20090414 In: Human genetics vol. 125 Availability: No items available. Save to lists Add to cart (remove)
	5.	HLA-DRB1 allele frequency and immunological response in obstructive sleep apnea syndrome in Turkish population. [electronic resource] by Tepebaşı, Muhammet Yusuf Şahin Calapoğlu, Nilüfer Öztürk, Önder Sancer, Okan Gonca, Taner Producer: 20190206 In: The clinical respiratory journal vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Analysis of the alpha-1-antitrypsin deficient alleles M3S, MZ, and ZZ by biochemical and molecular methods: a family study. [electronic resource] by Calapoğlu, Mustafa Değer, Orhan Balaban, Fulya Sahin Calapoğlu, Nilufer Bülbül, Yilmaz Burling, Keith Producer: 20090226 In: Biochemical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Serotonin transporter bi- and triallelic genotypes and their relationship with anxiety and academic performance: a preliminary study. [electronic resource] by Calapoğlu, Mustafa Sahin-Calapoğlu, Nilufer Karaçöp, Ataman Soyöz, Mustafa Elyıldırım, Umit Y Avşaroğlu, Selahattin Producer: 20110525 In: Neuropsychobiology vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein. [electronic resource] by Wattenhofer, Marie Sahin-Calapoglu, Nilüfer Andreasen, Ditte Kalay, Ersan Caylan, Refik Braillard, Bastien Fowler-Jaeger, Nicole Reymond, Alexandre Rossier, Bernard C Karaguzel, Ahmet Antonarakis, Stylianos E Producer: 20051110 In: Human genetics vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)