The Ultrasound and Genetic Characteristics of Fetuses With Laterality Defects—A Prenatal Cohort in Asian Population
Fuente:
Wiley Open Access
Saved in:
| Main Authors: | Wu Yi, Hua Renyi, Chen Yiyao, Wang Xiao, Chen Ping, Wang YanLin, Wang Hui |
|---|---|
| Format: | Artículo Open Access |
| Published: |
Wiley
2025
|
| Subjects: | |
| Online Access: | |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
Prenatal Diagnosis of Arthrogryposis Multiplex Congenita (AMC): Ultrasound and Genetic Findings in 69 Fetuses From 67 Unrelated Families
by: Tingting Yao, et al.
Published: (2026)
by: Tingting Yao, et al.
Published: (2026)
Optical Genome Mapping for Prenatal Diagnosis in Fetuses With Structural Anomalies
by: Yiyun Xu, et al.
Published: (2025)
by: Yiyun Xu, et al.
Published: (2025)
Prenatal Exome Sequencing Analysis in Fetuses With Structural Anomalies: A Multicenter Prospective Cohort Study With Practical Implications
by: Yulin Jiang, et al.
Published: (2025)
by: Yulin Jiang, et al.
Published: (2025)
Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia
by: Yan Lü, et al.
Published: (2024)
by: Yan Lü, et al.
Published: (2024)
Clinical and Molecular Features of Ciliopathies Diagnosed by Prenatal Exome Sequencing in Fetuses With Ultrasound Abnormalities
by: Xiaofan Zhu, et al.
Published: (2025)
by: Xiaofan Zhu, et al.
Published: (2025)
Integrating the Continuum of Genetic Testing From Fetus to Neonate: A Review of Prenatal Genetic Testing and the Overlap With Newborn Testing
by: Sarah Harris, et al.
Published: (2025)
by: Sarah Harris, et al.
Published: (2025)
Prenatal Phenotype of a Heterozygous Missense CHD4 Variant in a Fetus With Widened Cerebral Subarachnoid Space, Increased Head Circumference and Polyhydramnios
by: Fan Zhou, et al.
Published: (2025)
by: Fan Zhou, et al.
Published: (2025)
Genetic Investigation of Fetuses With Isolated Unilateral Renal Agenesis Identified on Second Trimester Ultrasound: A Single Referral Center Experience
by: Yong‐Ling Zhang, et al.
Published: (2025)
by: Yong‐Ling Zhang, et al.
Published: (2025)
Prenatal Phenotypic Expansion: A Fetus With Neurodegeneration With Developmental Delay, Early Respiratory Failure, Myoclonic Seizures, and Brain Abnormalities (NDDRSB) and MED11 Variants
by: Cong Zhou, et al.
Published: (2024)
by: Cong Zhou, et al.
Published: (2024)
Can Prenatal Ultrasound and Genetic Testing Reliably Exclude Non‐Isolated Clubfoot?
by: Jana M. de Vries, et al.
Published: (2025)
by: Jana M. de Vries, et al.
Published: (2025)
Prenatal Ultrasound Observations and Postnatal Manifestations Linked to PIGW Variants
by: Xin Chen, et al.
Published: (2025)
by: Xin Chen, et al.
Published: (2025)
Clinically Significant Genetic Results in Fetuses With Isolated Horseshoe Kidney
by: Qiu‐Xia Yu, et al.
Published: (2026)
by: Qiu‐Xia Yu, et al.
Published: (2026)
Prenatal Diagnosis of Caroli's Disease by Ultrasound and MRI Imaging
by: Ying‐Li Wei, et al.
Published: (2025)
by: Ying‐Li Wei, et al.
Published: (2025)
Genetic Investigation of Fetal Left‐Right Laterality Defects Identified in the Second Trimester of Pregnancy
by: Qiu‐Xia Yu, et al.
Published: (2026)
by: Qiu‐Xia Yu, et al.
Published: (2026)
Low‐Pass Genome Sequencing Reveals Associations Between Chromosomal Aberrations and Ultrasonographic Anomalies in a Cohort of 19,452 Fetuses
by: Lijuan Pan, et al.
Published: (2026)
by: Lijuan Pan, et al.
Published: (2026)
Prenatal Screening for Fetal X‐Linked Ichthyosis: A Large Cohort Study Combining Non‐Invasive Prenatal Testing and Maternal Serum Unconjugated Estriol Analysis
by: Miao Han, et al.
Published: (2026)
by: Miao Han, et al.
Published: (2026)
Longitudinal Magnetic Resonance Imaging Study of Hemodynamic Changes in the Third Trimester in Fetuses With Major Congenital Heart Defects and Healthy Fetuses
by: Signe G. Hellmuth, et al.
Published: (2025)
by: Signe G. Hellmuth, et al.
Published: (2025)
Application of Genetic Origin Analysis of Copy Number Variations in Non‐Invasive Prenatal Testing
by: Jing Wang, et al.
Published: (2024)
by: Jing Wang, et al.
Published: (2024)
Prenatal Ultrasound in the Diagnosis of Anorectal Malformations: Correlating Prenatal Signs With Postnatal Outcomes
by: D. Huijgen, et al.
Published: (2024)
by: D. Huijgen, et al.
Published: (2024)
Whole Exome Sequencing in a Population of Fetuses With Structural Anomalies
by: Natalie Burrill, et al.
Published: (2025)
by: Natalie Burrill, et al.
Published: (2025)
Risk of Genetic Abnormality in Fetuses With Unilateral Versus Bilateral Pleural Effusions
by: Brian Burnett, et al.
Published: (2024)
by: Brian Burnett, et al.
Published: (2024)
Prenatal and Perinatal Outcomes in Fetuses With Macrocystic Congenital Pulmonary Airway Malformations: Thoracoamniotic Shunting Versus Expectant Management
by: Laurence Sophie Carmant, et al.
Published: (2026)
by: Laurence Sophie Carmant, et al.
Published: (2026)
Placental and Fetal Brain Volumes in Congenital Heart Disease Are Smallest Among Fetuses With Genetic Abnormalities
by: Sonali Ajwani, et al.
Published: (2025)
by: Sonali Ajwani, et al.
Published: (2025)
A Novel Homozygous Frameshift Variant in the FLVCR1 Gene Is Associated With Prenatal Microcephaly, Multiple Brain Structural Anomalies, and Abnormal Foot Posture
by: Jing Chen, et al.
Published: (2025)
by: Jing Chen, et al.
Published: (2025)
Differences in Prenatal and Postnatal Phenotypic Evaluations in Patients With Congenital Anomalies and Known Genetic Diagnoses
by: Nicole Horton, et al.
Published: (2025)
by: Nicole Horton, et al.
Published: (2025)
Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS Anomaly
by: Hadas Miremberg, et al.
Published: (2024)
by: Hadas Miremberg, et al.
Published: (2024)
Exome Sequencing in Fetuses With Bilateral Renal Agenesis Identified on Second Trimester Ultrasound: A Single Referral Center Experience
by: Qiu‐Xia Yu, et al.
Published: (2024)
by: Qiu‐Xia Yu, et al.
Published: (2024)
Advances and Challenges in Prenatal Detection and Genetic Diagnosis of Upper Limb Anomalies: Analysis of a South London and Kent Cohort
by: Federica Ruscitti, et al.
Published: (2024)
by: Federica Ruscitti, et al.
Published: (2024)
Prenatal Ultrasound Features of Biliary Atresia: Diagnostic Significance of Abnormal Gallbladder Size and Hepatic Hilar Cyst
by: Wu Xu, et al.
Published: (2025)
by: Wu Xu, et al.
Published: (2025)
Prenatal Diagnosis of Verheij Syndrome Associated With PUF60 Variants Presented With Ventricular Septal Defect and Scoliosis Identified by First Trimester Ultrasound
by: Ru Li, et al.
Published: (2025)
by: Ru Li, et al.
Published: (2025)
Prenatal Diagnosed Agenesis of the Corpus Callosum: Identifying the Underlying Genetic Etiologies
by: Xing Wei, et al.
Published: (2024)
by: Xing Wei, et al.
Published: (2024)
A Prospective Evaluation of the Diagnostic Utility for Low‐Coverage Genome Sequencing in Prenatal Samples: A Comparison With Chromosomal Microarray Analysis
by: Yan Yin, et al.
Published: (2025)
by: Yan Yin, et al.
Published: (2025)
Exome Sequencing of Fetuses With Intracranial Hemorrhage Unravels Novel Causative Genes and an Extreme Genetic Heterogeneity
by: Thibault Coste, et al.
Published: (2025)
by: Thibault Coste, et al.
Published: (2025)
Hydrops, Arthrogryposis, and Cerebellar Hypoplasia in a Fetus With a de Novo BICD2 Variant: Expanding the Prenatal Phenotype of SMALED2B
by: Francesca Romana Lepri, et al.
Published: (2025)
by: Francesca Romana Lepri, et al.
Published: (2025)
Microcephaly, Cerebellar Hypoplasia, Enlarged Posterior Fossa and Polyhydramnios: Prenatal Phenotypes for CASK‐ Related Disorders
by: Jing Chen, et al.
Published: (2025)
by: Jing Chen, et al.
Published: (2025)
Can Fetal Heterotaxy Syndrome Be Diagnosed Through Prenatal Ultrasound in the First Trimester (GA 11+0−13+6 Weeks)?
by: Biying Huang, et al.
Published: (2025)
by: Biying Huang, et al.
Published: (2025)
Prenatal exome sequencing for the morphologically normal fetus: Should we be doing it?
by: Zhi Gao, et al.
Published: (2024)
by: Zhi Gao, et al.
Published: (2024)
Quality of Evidence for Prenatal Down Syndrome Screening: An Umbrella Review
by: Yuehua Zhang, et al.
Published: (2026)
by: Yuehua Zhang, et al.
Published: (2026)
Contribution of Genomic Imbalance in Prenatal Congenital Anomalies of the Kidney and Urinary Tract: A Multi‐Center Cohort Study
by: Keying Li, et al.
Published: (2024)
by: Keying Li, et al.
Published: (2024)
Theoretical Performance of Comprehensive Non‐Invasive Prenatal Screening in Congenital Heart Defects
by: Emily Yang, et al.
Published: (2026)
by: Emily Yang, et al.
Published: (2026)
Similar Items
-
Prenatal Diagnosis of Arthrogryposis Multiplex Congenita (AMC): Ultrasound and Genetic Findings in 69 Fetuses From 67 Unrelated Families
by: Tingting Yao, et al.
Published: (2026) -
Optical Genome Mapping for Prenatal Diagnosis in Fetuses With Structural Anomalies
by: Yiyun Xu, et al.
Published: (2025) -
Prenatal Exome Sequencing Analysis in Fetuses With Structural Anomalies: A Multicenter Prospective Cohort Study With Practical Implications
by: Yulin Jiang, et al.
Published: (2025) -
Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia
by: Yan Lü, et al.
Published: (2024) -
Clinical and Molecular Features of Ciliopathies Diagnosed by Prenatal Exome Sequencing in Fetuses With Ultrasound Abnormalities
by: Xiaofan Zhu, et al.
Published: (2025)