Committee Opinion No. 581
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Obstetrics and Gynaecology
Reference13 articles.
1. Diagnostic Genome Profiling in Mental Retardation
2. Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation
3. Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations
4. Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases
5. Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting
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1. Genetic analysis of pregnancy loss and fetal structural anomalies by whole exome sequencing;Orphanet Journal of Rare Diseases;2024-09-09
2. Idiopathic polyhydramnios and postnatal outcomes of children: The role of exome sequencing;Prenatal Diagnosis;2024-04-29
3. Exploring the factors affecting classification and reporting of uncertain prenatal microarray findings, using a “virtual fetus” model‐a pilot study;Prenatal Diagnosis;2024-02-14
4. Diagnostic and prognostic role of soft ultrasound markers in prenatal detection and assessment of foetal abnormalities;Menopausal Review;2024
5. Chromosomal Microarray Analysis in Fetuses With Ultrasonographic Soft Markers: A Meta-Analysis of the Current Evidence;Journal of Korean Medical Science;2024
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