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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
di: Dana Brabbing‐Goldstein, et al.
Pubblicazione: (2024)

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

Transforming Prenatal Care in a Highly Inbred Population: Impact of a Multidisciplinary Board
di: Abdullah H. Alfalah, et al.
Pubblicazione: (2026)

Variation in the Genetic Workup of Polyhydramnios: An International and Inter‐Specialty Survey
di: Roni Zemet, et al.
Pubblicazione: (2026)

Moderate Diagnostic Yield of Exome Sequencing in Fetal Growth Restriction: Retrospective Insights
di: Maud Langeois, et al.
Pubblicazione: (2026)

Fetal Sylvian Fissure Maturation in Congenital Heart Disease and Its Relation to Expected Brain Arterial Oxygen Saturation: A Longitudinal Study
di: Xiaowei Xiong, et al.
Pubblicazione: (2026)

Monopolar Single Tip Radiofrequency as Treatment of Giant Placental Chorioangioma
di: Grégoire Dumery, et al.
Pubblicazione: (2026)

Intrauterine Transfusions in Fetuses Affected by Parvovirus B19: Complications, Challenges and Outcomes
di: Banu Özbakir, et al.
Pubblicazione: (2026)

Genetic Investigation of Fetal Left‐Right Laterality Defects Identified in the Second Trimester of Pregnancy
di: Qiu‐Xia Yu, et al.
Pubblicazione: (2026)

Prenatal Diagnosis of Posterior Urethral Valves: Timing of Diagnosis and Mid‐Term Renal Function When Second and Third Trimester Ultrasounds Are Systematically Performed
di: Silvia Pecorelli, et al.
Pubblicazione: (2026)

Multicentre Evaluation of Perinatal Outcomes After Selective Feticide in Dichorionic Twins in Italy
di: Mariano Lanna, et al.
Pubblicazione: (2026)

In Vivo Effect of a Synthetic Amniotic Fluid on Fetal Lung and Gastrointestinal Tract: A Pre‐Clinical Rodent Model
di: Braxton Forde, et al.
Pubblicazione: (2026)

Reproductive Decision‐Making Among BRCA1/2 Pathogenic Variants Carriers and Physicians: Attitudes Toward Preimplantation and Prenatal Genetic Testing
di: Marta D'Alonzo, et al.
Pubblicazione: (2026)

Evaluation of Maternal Safety Following Prenatal Cell and Gene Therapy for Hemophilia A
di: Quan Minh Pham, et al.
Pubblicazione: (2026)

Clinically Significant Genetic Results in Fetuses With Isolated Horseshoe Kidney
di: Qiu‐Xia Yu, et al.
Pubblicazione: (2026)

Response to Commentary on “Virtual Reality Simulation in Teaching Fetoscopic Laser Placental Photocoagulation in Twin‐To‐Twin Transfusion Syndrome”
di: Catherine Windrim, et al.
Pubblicazione: (2026)

Attitudes Toward Prenatal Interventions in the Fanconi Anemia Community
di: Tony Lum, et al.
Pubblicazione: (2026)

Severe Nonketotic Hyperglycinemia in Twins Caused by GLDC Variants: The Importance of Accurate Prenatal Variant Interpretation, Counseling, and VUS Disclosure
di: Christopher Connolly, et al.
Pubblicazione: (2026)

A Framework for Bioinformatic Reporting in Prenatal Sequencing: Insights From a Systematic Review
di: Ashley J. Pritchard, et al.
Pubblicazione: (2026)