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Potentially Missed Diagnoses in Prenatal Versus Postnatal Exome Sequencing in the Lack of Informative Phenotype: Lessons Learned From a Postnatal Cohort
por: Dana Brabbing‐Goldstein, et al.
Publicado: (2024)

Prenatal Screening Via cfDNA – Paired‐End Sequencing Utilizing Fragment Size Information Reduces the Screen Positive Rate for X Chromosome Aneuploidies
por: Susan Hancock, et al.
Publicado: (2026)

Spinal Muscular Atrophy Carrier Screening: Assessment of Provider Knowledge and Clinical Practice
por: Melissa Riegel, et al.
Publicado: (2025)

In‐Utero Therapy for Fetal Vascular Anomalies: Efficacy and Tolerance of Sirolimus Administered to the Pregnant Patient
por: Ionela Iacobas, et al.
Publicado: (2025)

Prenatal Ultrasound Features of Biliary Atresia: Diagnostic Significance of Abnormal Gallbladder Size and Hepatic Hilar Cyst
por: Wu Xu, et al.
Publicado: (2025)

Opportunities and Challenges of Fetal Gene Therapy
por: Médéric Jeanne, et al.
Publicado: (2025)

Assessment of Learning Curve for Radiofrequency Ablation in Twin Reversed Arterial Perfusion Sequence: A Simulation Model Study
por: Tanchanok Chaiperm, et al.
Publicado: (2025)

Prenatal Evaluation of Scrotal Masses: A Systematic Literature Review
por: Federica Romanzi, et al.
Publicado: (2025)

Performance of Prenatal Cell‐Free DNA Screening for Foetal Chromosome Aneuploidies and Microdeletion/Microduplication Syndromes: A Retrospective Study of 64,482 Consecutive Cases From a Prenatal Diagnosis Centre in China
por: Feiyan Pan, et al.
Publicado: (2025)

Comparing the Introduction and Implementation of Noninvasive Prenatal Testing (NIPT) in Japan, the Netherlands, and the United States: An Integrative Review
por: Chloe Connor, et al.
Publicado: (2025)

A de novo WBP11 Pathogenic Variant in a Fetus With Cystic Brain Malformation and Growth Restriction
por: Gulvir Gill, et al.
Publicado: (2025)

Fetal Anogenital Distance Correlates With Hypospadias and Curvature Severity
por: Michael Frumer, et al.
Publicado: (2025)

Genome‐Wide Cell‐Free DNA Analysis for Aneuploidy Detection in Miscarriages: Test Performance Meta‐Analysis
por: Montse Pauta, et al.
Publicado: (2025)

Cell‐Free DNA Results Indicating Mosaic Monosomy X of Likely Maternal Origin: Impact on Genetic Counseling Practices and Patient Experiences
por: Audrey McBride, et al.
Publicado: (2025)

Whole Exome Sequencing in a Population of Fetuses With Structural Anomalies
por: Natalie Burrill, et al.
Publicado: (2025)

Genome Sequencing for All Pregnant Persons: Navigating the Next Frontier in Prenatal Diagnosis Through Patient Reflections
por: Kristen E. Kelly, et al.
Publicado: (2025)

Can Prenatal Ultrasound and Genetic Testing Reliably Exclude Non‐Isolated Clubfoot?
por: Jana M. de Vries, et al.
Publicado: (2025)

Microcephaly, Cerebellar Hypoplasia, Enlarged Posterior Fossa and Polyhydramnios: Prenatal Phenotypes for CASK‐ Related Disorders
por: Jing Chen, et al.
Publicado: (2025)

Fetal Endoscopic Tracheal Occlusion (FETO) for Left and Right Congenital Diaphragmatic Hernia in Canada
por: Yada Kunpalin, et al.
Publicado: (2025)