Elena Papageorgiou
Athens, ESYE31 11528, Greece
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
Association of Waardenburg syndrome with a new mutation in the PAX3 gene: A case report and literature review.
Journal: Biomedical reports
Published: November 10, 2024
Novel familial KDF1 mutation detected in members of a three-generation family with clinical manifestations of ectodermal dysplasia: A report of four cases.
Journal: Biomedical reports
Published: July 15, 2024
The Effect of Resolution Level and Targeted Design in the Diagnostic Performance of Prenatal Chromosomal Microarray Analysis.
Journal: Fetal diagnosis and therapy
Published: November 04, 2022
A novel familial mutation associated with Treacher Collins syndrome: A case report.
Journal: Biomedical reports
Published: February 07, 2019
Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study.
Journal: Prenatal diagnosis
Published: October 14, 2016
Prenatal diagnosis of 1p34.3 interstitial microdeletion by aCGH in a fetus with jaw bone abnormalities.
Journal: Molecular cytogenetics
Published: July 27, 2016
Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay.
Journal: Cytogenetic and genome research
Published: March 03, 2015
Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases.
Journal: Prenatal diagnosis
Published: February 09, 2015
Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH.
Journal: Molecular cytogenetics
Published: August 07, 2013
Showing 1-9 of 9
Last Updated: 09/26/2026