Thyroid diseases articles within European Journal of Human Genetics

Featured

• Article | 18 February 2020

  Primrose syndrome: a phenotypic comparison of patients with a ZBTB20 missense variant versus a 3q13.31 microdeletion including ZBTB20

  • Aurélien Juven
  • , Sophie Nambot
  •  & Laurence Faivre

• Article | 20 April 2011

  Nasal speech and hypothyroidism are common hallmarks of 12q15 microdeletions

  • Sarah Vergult
  • , Danijela Krgovic
  •  & Björn Menten