Cavdarli, B. Et Al. 2018. Whole exome sequencing identifies a novel mutation in ADCY5 in a patient with developmental delay and dystonia. 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) , (Milan, Italy), 317.

Cavdarli, B., Esen, N., Topcu, V., Aksoy, A., Danis, A., & Anlar, B., (2018). Whole exome sequencing identifies a novel mutation in ADCY5 in a patient with developmental delay and dystonia . 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) (pp.317). Milan, Italy

Cavdarli, B. Et Al. "Whole exome sequencing identifies a novel mutation in ADCY5 in a patient with developmental delay and dystonia," 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

Cavdarli, B. Et Al. "Whole exome sequencing identifies a novel mutation in ADCY5 in a patient with developmental delay and dystonia." 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.317, 2018

Cavdarli, B. Et Al. (2018) . "Whole exome sequencing identifies a novel mutation in ADCY5 in a patient with developmental delay and dystonia." 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) , Milan, Italy, p.317.

@conferencepaper{conferencepaper, author={B. Cavdarli Et Al. }, title={Whole exome sequencing identifies a novel mutation in ADCY5 in a patient with developmental delay and dystonia}, 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={317} }