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	1.	Identification of an ancestral haplotype of the 35delG mutation in the GJB2 (connexin 26) gene responsible for autosomal recessive non-syndromic hearing loss in families from the Eastern Black Sea Region in Turkey. [electronic resource] by Balci, Burcu Gerçeker, Filiz Ozbaş Aksoy, Songül Sennaroğlu, Gonca Kalay, Ersan Sennaroğlu, Levent Dinçer, Pervin Producer: 20051115 In: The Turkish journal of pediatrics vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	2.	L-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1. [electronic resource] by Topçu, Meral Jobard, Florence Halliez, Sophie Coskun, Turgay Yalçinkayal, Cengiz Gerceker, Filiz Ozbas Wanders, Ronald J A Prud'homme, Jean-François Lathrop, Mark Ozguc, Meral Fischer, Judith Producer: 20060112 In: Human molecular genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycan. [electronic resource] by Dinçer, Pervin Balci, Burcu Yuva, Yeliz Talim, Beril Brockington, Martin Dinçel, Deniz Torelli, Silvia Brown, Sue Kale, Gülsev Haliloglu, Göknur Gerçeker, Filiz Ozbas Atalay, Rengül Cetin Yakicier, Cengiz Longman, Cheryl Muntoni, Francesco Topaloglu, Haluk Producer: 20040226 In: Neuromuscular disorders : NMD vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)