Incidence and spectrum of chromosome abnormalities in miscarriage samples: a retrospective study of 330 cases

C Gug, A Rațiu, D Navolan, I Drăgan… - … and Genome Research, 2019 - karger.com
Embryonic chromosome abnormalities are the most important causes of early spontaneous
abortions. The aim of this study was to evaluate the spectrum and the frequencies of …

Polyploidy in First and Second Trimester Pregnancies in Romania-a Retrospective Study.

C Gug, F Burada, M Ioana, AL Riza… - Clinical …, 2020 - search.ebscohost.com
Background: Polyploidy is a rare lethal cytogenetic anomaly in pregnancies, generally
leading to pregnancy termination. This study aims to compare first and second trimester …

CHARGE syndrome associated with de novo (I1460Rfs* 15) frameshift mutation of CHD7 gene in a patient with arteria lusoria and horseshoe kidney

C Gug, EV Gorduza, A Lăcătuşu… - Experimental and …, 2020 - spandidos-publications.com
CHARGE syndrome is an autosomal dominant condition caused by mutations in the
chromodomain helicase DNA binding protein 7 (CHD7) gene. The present study reported on …

A 10-YEAR STUDY OF CHILDREN WITH GONADAL TUMORS AND DISORDERS OF SEX DIFFERENTIATION, IN ROMANIA

U Ataikiru, R Iacob, A Chirita-Emandi… - Acta …, 2024 - pmc.ncbi.nlm.nih.gov
Context Children having gonadal tumors and disorder of sex differentiation (DSD) are rare.
Objective To investigate the presentation of DSD children with malignant gonadal tumors …