A new recognizable recessive syndrome with distinct dysmorphism, lymphedema and sensorineural hearing loss caused by Carboxypeptidase D mutations

Kayserili H., Altunoglu U., Laupheimer S., Bonnard C., Reversade B.

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.464 identifier

  • Publication Type: Conference Paper / Summary Text
  • Volume: 26
  • City: Copenhagen
  • Country: Denmark
  • Page Numbers: pp.464
  • Istanbul University Affiliated: Yes