Rare structural chromosomal abnormalities in prenatal diagnosis; clinical and cytogenetic findings on 10125 prenatal cases.

doi:10.5146/tjpath.2014.01280

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Article

Rare structural chromosomal abnormalities in prenatal diagnosis; clinical and cytogenetic findings on 10125 prenatal cases.

Turk patoloji dergisi - 1 Jan 2015

Yakut Sezin, Çetin Zafer, Şİmşek Mehmet, Mendilcioğlu Ibrahim Inanç, Toru Havva Serap, Berker Karaüzüm Sibel, Lüleci Güven

Abstract excerpt

UNLABELLED: Objective: The aim of this study was presentation of the ultrasonographic findings and perinatal autopsy of cases with rare chromosomal abnormalities. MATERIAL AND METHOD: A total of 10125 prenatal cases over 17 years including 8731 amniocentesis, 973 chorionic villus sampling, and 421 fetal blood sampling cases were evaluated for prenatal cytogenetic diagnosis. Conventional cytogenetic studies,...

Topics

Amniocentesis
Autopsy
Chromosome Aberrations
Chromosome Disorders
Comparative Genomic Hybridization
Female
Genetic Testing
Genotype
Humans
In Situ Hybridization, Fluorescence

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Phenotype

Predictive Value of Tests

Pregnancy

Prenatal Diagnosis

Turkey

Ultrasonography, Prenatal

Source

Open in PubMed

Identifiers

PMID: 25301051
DOI: 10.5146/tjpath.2014.01280

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