AKALIN, İ. Et Al. 2016. A novel homozygous IFT122 p I460N c 1379T A mutation inSensenbrenner syndrome a rare disorder within two cousins. ESHG kongresi .

AKALIN, İ., ELÇİOĞLU, H. N., CANDAN, C., YILMAZ, S., & Yücetürk, B., (2016). A novel homozygous IFT122 p I460N c 1379T A mutation inSensenbrenner syndrome a rare disorder within two cousins . ESHG kongresi

AKALIN, İBRAHİM Et Al. "A novel homozygous IFT122 p I460N c 1379T A mutation inSensenbrenner syndrome a rare disorder within two cousins," ESHG kongresi, 2016

AKALIN, İBRAHİM Et Al. "A novel homozygous IFT122 p I460N c 1379T A mutation inSensenbrenner syndrome a rare disorder within two cousins." ESHG kongresi , 2016

AKALIN, İ. Et Al. (2016) . "A novel homozygous IFT122 p I460N c 1379T A mutation inSensenbrenner syndrome a rare disorder within two cousins." ESHG kongresi .

@conferencepaper{conferencepaper, author={İBRAHİM AKALIN Et Al. }, title={A novel homozygous IFT122 p I460N c 1379T A mutation inSensenbrenner syndrome a rare disorder within two cousins}, congress name={ESHG kongresi}, city={}, country={}, year={2016}}