H. Kayserili Et Al. , "A new recognizable recessive syndrome with distinct dysmorphism, lymphedema and sensorineural hearing loss caused by Carboxypeptidase D mutations," 50th European-Society-of-Human-Genetics (ESHG) Conference , vol.26, Copenhagen, Denmark, pp.464, 2017
Kayserili, H. Et Al. 2017. A new recognizable recessive syndrome with distinct dysmorphism, lymphedema and sensorineural hearing loss caused by Carboxypeptidase D mutations. 50th European-Society-of-Human-Genetics (ESHG) Conference , (Copenhagen, Denmark), 464.
Kayserili, H., Altunoglu, U., Laupheimer, S., Bonnard, C., & Reversade, B., (2017). A new recognizable recessive syndrome with distinct dysmorphism, lymphedema and sensorineural hearing loss caused by Carboxypeptidase D mutations . 50th European-Society-of-Human-Genetics (ESHG) Conference (pp.464). Copenhagen, Denmark
Kayserili, H. Et Al. "A new recognizable recessive syndrome with distinct dysmorphism, lymphedema and sensorineural hearing loss caused by Carboxypeptidase D mutations," 50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 2017
Kayserili, H. Et Al. "A new recognizable recessive syndrome with distinct dysmorphism, lymphedema and sensorineural hearing loss caused by Carboxypeptidase D mutations." 50th European-Society-of-Human-Genetics (ESHG) Conference , Copenhagen, Denmark, pp.464, 2017
Kayserili, H. Et Al. (2017) . "A new recognizable recessive syndrome with distinct dysmorphism, lymphedema and sensorineural hearing loss caused by Carboxypeptidase D mutations." 50th European-Society-of-Human-Genetics (ESHG) Conference , Copenhagen, Denmark, p.464.
@conferencepaper{conferencepaper, author={H. Kayserili Et Al. }, title={A new recognizable recessive syndrome with distinct dysmorphism, lymphedema and sensorineural hearing loss caused by Carboxypeptidase D mutations}, congress name={50th European-Society-of-Human-Genetics (ESHG) Conference}, city={Copenhagen}, country={Denmark}, year={2017}, pages={464} }