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Browsing by Author Toraman, B.

Full Text	Issue Date	Title	Author(s)
	2011	CEP152 is a genome maintenance protein disrupted in Seckel syndrome	Kalay, E.; Yigit, G.; Aslan, Y.; Brown, K.E.; Pohl, E., et al
	2007	Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.	Collin, R.W.J.; Kalay, E.; Oostrik, J.; Caylan, R.; Wollnik, B., et al