Akdeniz, B. Et Al. 2018. Severe speech delay in Cohen Syndrome: three novel mutations and the long-term follow-up of nine patients. 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) , (Milan, Italy), 315-316.

Akdeniz, B., Gunes, N., ULUDAĞ, D., Ercan-Sencicek, G., ÇAĞLAYAN, A. O., Bilguvar, K., ... TÜYSÜZ, B.(2018). Severe speech delay in Cohen Syndrome: three novel mutations and the long-term follow-up of nine patients . 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) (pp.315-316). Milan, Italy

Akdeniz, B. Et Al. "Severe speech delay in Cohen Syndrome: three novel mutations and the long-term follow-up of nine patients," 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 2018

Akdeniz, B. Et Al. "Severe speech delay in Cohen Syndrome: three novel mutations and the long-term follow-up of nine patients." 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) , Milan, Italy, pp.315-316, 2018

Akdeniz, B. Et Al. (2018) . "Severe speech delay in Cohen Syndrome: three novel mutations and the long-term follow-up of nine patients." 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) , Milan, Italy, pp.315-316.

@conferencepaper{conferencepaper, author={B. Akdeniz Et Al. }, title={Severe speech delay in Cohen Syndrome: three novel mutations and the long-term follow-up of nine patients}, congress name={51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)}, city={Milan}, country={Italy}, year={2018}, pages={315-316} }