Login / Signup

Cytogenetic and molecular characterization of a patient having infertility and mild intellectual disability with a very rare unstable ring chromosome 13.

Murat KayaIlknur SuerTugba KalayciBirsen KaramanSukru OzturkSukru Palanduz
Published in: Scottish medical journal (2022)
gene, in particular, may explain our patient's MID, and the other deleted genes at 13q34 may explain our patient's infertility.
Keyphrases
  • intellectual disability
  • case report
  • autism spectrum disorder
  • genome wide
  • copy number
  • type diabetes
  • gene expression
  • genome wide identification
  • adipose tissue
  • insulin resistance