Your browser doesn't support javascript.
loading
Correction to: A mutation in NOTCH2 gene first associated with Hajdu-Cheney syndrome in a Greek family: diversity in phenotype and response to treatment.
Efstathiadou, Zoe A; Kostoulas, Charilaos; Polyzos, Stergios A; Adamidou, Fotini; Georgiou, Ioannis; Kita, Marina.
Affiliation
  • Efstathiadou ZA; Department of Endocrinology, "Hippokration" General Hospital of Thessaloniki, Thessaloniki, Greece. zefsta@endo.gr.
  • Kostoulas C; Laboratory of Medical Genetics in Clinical Practice, Faculty of Medicine, University of Ioannina, Ioannina, Greece.
  • Polyzos SA; First Laboratory of Pharmacology, School of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
  • Adamidou F; Department of Endocrinology, "Hippokration" General Hospital of Thessaloniki, Thessaloniki, Greece.
  • Georgiou I; Laboratory of Medical Genetics in Clinical Practice, Faculty of Medicine, University of Ioannina, Ioannina, Greece.
  • Kita M; Department of Endocrinology, "Hippokration" General Hospital of Thessaloniki, Thessaloniki, Greece.
Endocrine ; 70(3): 659-660, 2020 Dec.
Article in En | MEDLINE | ID: mdl-33025564
ABSTRACT
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: Endocrine Journal subject: ENDOCRINOLOGIA Year: 2020 Document type: Article Affiliation country: Grecia
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: Endocrine Journal subject: ENDOCRINOLOGIA Year: 2020 Document type: Article Affiliation country: Grecia