Topf, A. Et Al. 2019. Severe neurodevelopmental disease caused by a homozygous TLK2 variant. 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , (Gothenburg, Sweden), 1850-1851.

Topf, A., Oktay, Y., Balaraju, S., Yilmaz, E., Sonmezler, E., Yis, U., ... Laurie, S.(2019). Severe neurodevelopmental disease caused by a homozygous TLK2 variant . 52nd Conference of the European-Society-of-Human-Genetics (ESHG) (pp.1850-1851). Gothenburg, Sweden

Topf, A. Et Al. "Severe neurodevelopmental disease caused by a homozygous TLK2 variant," 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, Sweden, 2019

Topf, A. Et Al. "Severe neurodevelopmental disease caused by a homozygous TLK2 variant." 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , Gothenburg, Sweden, pp.1850-1851, 2019

Topf, A. Et Al. (2019) . "Severe neurodevelopmental disease caused by a homozygous TLK2 variant." 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , Gothenburg, Sweden, pp.1850-1851.

@conferencepaper{conferencepaper, author={A. Topf Et Al. }, title={Severe neurodevelopmental disease caused by a homozygous TLK2 variant}, congress name={52nd Conference of the European-Society-of-Human-Genetics (ESHG)}, city={Gothenburg}, country={Sweden}, year={2019}, pages={1850-1851} }