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The Journal of Maternal-Fetal & Neonatal Medicine, ISSN 1476-7058, 01/2017, Volume 30, Issue 2, pp. 194 - 198
Journal Article
British Journal of Haematology, ISSN 0007-1048, 05/2005, Volume 129, Issue 4, pp. 520 - 530
Journal Article
Molecular Cytogenetics, ISSN 1755-8166, 04/2014, Volume 7, Issue 1, pp. 26 - 26
Background: Array-based comparative genomic hybridization possesses a number of significant advantages over conventional cytogenetic and other molecular... 
Array-based CGH | Submicroscopic chromosomal abnormalities | Prenatal diagnostics | MALFORMATIONS | PREGNANCIES | ULTRASOUND | GENETICS & HEREDITY | DEL(18P) SYNDROME | FETUSES | COMPARATIVE GENOMIC HYBRIDIZATION | ABERRATIONS | EXPRESSION | Comparative analysis | Instrument industry
Journal Article
Journal Article
Journal of Obstetrics and Gynaecology, ISSN 0144-3615, 05/2018, Volume 38, Issue 4, pp. 498 - 501
The aim of this study was to evaluate which chromosomal abnormalities in our cohort of foetuses with increased nuchal translucency (NT) in the first trimester... 
Nuchal translucency | prenatal diagnosis | cell free DNA screening | submicroscopic chromosomal abnormalities | chromosomal microarray analysis | ARRAY | METAANALYSIS | MICROARRAY | SUBMICROSCOPIC CHROMOSOMAL-ABNORMALITIES | OBSTETRICS & GYNECOLOGY | NORMAL KARYOTYPE | MATERNAL PLASMA | ULTRASOUND | PREGNANCIES | DISORDER | PRENATAL-DIAGNOSIS
Journal Article
FRONTIERS IN GENETICS, ISSN 1664-8021, 08/2019, Volume 10, p. 761
Background: Increased nuchal translucency (NT) is an important biomarker associated with increased risk of fetal structural anomalies. It is known to be... 
genomic variants | structural rearrangement | increased nuchal translucency | ARRAY | ASSAY | VARIANTS | GENETICS & HEREDITY | genome sequencing | prenatal diagnosis | SUBMICROSCOPIC CHROMOSOMAL-ABNORMALITIES
Journal Article
Journal Article
Journal Article
Journal Article
Pediatric Research, ISSN 0031-3998, 2009, Volume 66, Issue 4, pp. 357 - 363
Momentum around the era of genomic medicine is building, and with it, anticipation of the benefits that whole genome analysis (personalized or individualized... 
GENETICS | LEGAL | AUTISM SPECTRUM DISORDER | PEDIATRICS | HYBRIDIZATION | SCIENCE | REARRANGEMENTS | STRUCTURAL VARIATION | SOCIETY | COPY-NUMBER VARIATION | SUBMICROSCOPIC CHROMOSOMAL-ABNORMALITIES | Microarray Analysis - methods | Diagnosis, Differential | Genetic Testing | Genetics, Medical | Humans | Genome, Human | Genomics - methods
Journal Article
Journal Article