Our research

Check the list of our publications

Whole-exome sequencing identifies homozygous GPR161 mutation in a family with pituitary stalk interruption syndrome

Downloads:

BibTeX:

 {%raw%}@article{karaca2014whole,
  title = {Whole-exome sequencing identifies homozygous GPR161 mutation in a family with pituitary stalk interruption syndrome},
  author = {Karaca, Ender and Buyukkaya, Ramazan and Pehlivan, Davut and Charng, Wu-Lin and Yaykasli, Kursat O and Bayram, Yavuz and Gambin, Tomasz and Withers, Marjorie and Atik, Mehmed M and Arslanoglu, Ilknur and others},
  journal = {The Journal of Clinical Endocrinology \& Metabolism},
  volume = {100},
  number = {1},
  pages = {E140--E147},
  year = {2014},
  publisher = {Endocrine Society Chevy Chase, MD},
  public = {yes}
}
{%endraw%}