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Application of chromosomal microarray to investigate genetic causes of isolated fetal growth restriction
- Source :
- Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-6 (2018), Molecular Cytogenetics
- Publication Year :
- 2018
- Publisher :
- BMC, 2018.
-
Abstract
- Background Application of chromosomal microarray analysis (CMA) to investigate the genetic characteristics of fetal growth restriction (FGR) without ultrasonic structural anomalies at 18–32 weeks. Methods This study includes singleton fetuses with the estimated fetal weight (EFW) using the formula of Hadlock C below the 10th percentile for gestational age. FGRs without structural anomalies were selected, and the ones at high risk of noninvasive prenatal testing for trisomy 13, 18 and 21 would be excluded. The cases were divided into two groups: early-onset group (
- Subjects :
- medicine.medical_specialty
lcsh:QH426-470
Prenatal diagnosis
Biochemistry
03 medical and health sciences
0302 clinical medicine
Genetics
Medicine
030212 general & internal medicine
Copy-number variation
Molecular Biology
Genetics (clinical)
Gynecology
Fetus
030219 obstetrics & reproductive medicine
business.industry
Research
Biochemistry (medical)
Fetal growth restriction
Cytogenetics
Uniparental disomy
Gestational age
Karyotype
medicine.disease
lcsh:Genetics
Molecular Medicine
Chromosomal microarray
business
Trisomy
Karyotype analysis
Subjects
Details
- Language :
- English
- ISSN :
- 17558166
- Volume :
- 11
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Molecular Cytogenetics
- Accession number :
- edsair.doi.dedup.....21d4b639e8eee579466d4378901f4ea9
- Full Text :
- https://doi.org/10.1186/s13039-018-0382-4