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Publications by Y. Arens

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

Ultrasound in Obstetrics and Gynecology

Nuclear Medicine

Ultrasound Technology

Reproductive Medicine

English

P02.04: Diagnosis of Herlyn-Werner-Wunderlich as a Result of Fetal Anomalies in the Second Trimester Scan

Ultrasound in Obstetrics and Gynecology

Nuclear Medicine

Ultrasound Technology

Reproductive Medicine

English

Related publications

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

Journal of Genetic Counseling

English

125: Whole Exome Sequencing (WES) in Prenatal Diagnosis for Carefully Selected Cases

American Journal of Obstetrics and Gynecology

English

Whole Exome Sequencing for Prenatal Diagnosis of CHARGE Syndrome: A Case Report

English

Parental Perceptions of Prenatal Whole Exome Sequencing (PPPWES) Study

Prenatal Diagnosis

English

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

Ultrasound in Obstetrics and Gynecology

Nuclear Medicine

Ultrasound Technology

Reproductive Medicine

English

Application of Whole Exome Sequencing in the Diagnosis of Hereditary Neurological Diseases

Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova

English

Whole Exome Sequencing in Monogenic Dyslipidemias

Journal of Atherosclerosis and Thrombosis

Internal Medicine

Cardiovascular Medicine

English

Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Clinical Application of Whole-Exome Sequencing

English