Balci, B. Et Al. 2005. 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. TURKISH JOURNAL OF PEDIATRICS , vol.47, no.3 , 213-221.

Balci, B., Gerceker, F., Aksoy, S., Sennaroglu, G., Kalay, E., Sennaroglu, L., ... Dincer, P. R.(2005). 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. TURKISH JOURNAL OF PEDIATRICS , vol.47, no.3, 213-221.

Balci, B Et Al. "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," TURKISH JOURNAL OF PEDIATRICS , vol.47, no.3, 213-221, 2005

Balci, B Et Al. "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." TURKISH JOURNAL OF PEDIATRICS , vol.47, no.3, pp.213-221, 2005

Balci, B. Et Al. (2005) . "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." TURKISH JOURNAL OF PEDIATRICS , vol.47, no.3, pp.213-221.

@article{article, author={B Balci Et Al. }, title={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}, journal={TURKISH JOURNAL OF PEDIATRICS}, year=2005, pages={213-221} }