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Fetal Axillary Cystic Lymphangioma Detected by Prenatal Ultrasonography

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Whole Exome Sequencing for Prenatal Diagnosis in Cases With Fetal Anomalies: Criteria to Improve Diagnostic Yield

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P05.10: Using Whole-Exome Sequencing in Prenatal Diagnosis of Severe Fetal Abnormalities

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Parental Perceptions of Prenatal Whole Exome Sequencing (PPPWES) Study

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OP01.09: Finding the Genomic Bases of Ultrasound-Detected Fetal Anomalies in First Trimester by Whole-Genome Sequencing

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EP13.07: Pathological Findings in the Study of Prenatal Arrays by Structural Ultrasound Anomalies

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Molecular Autopsy by Trio Exome Sequencing (ES) and Postmortem Examination in Fetuses and Neonates With Prenatally Identified Structural Anomalies

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OC20.02: Prenatal Diagnosis by Chromosome Microarray Analysis and Whole-Exome Sequencing for Fetuses With Skeletal Dysplasia

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EP08.05: Fetal Anomalies Detected in Sri Lankan Tertiary Fetal Medicine Referral Centre

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