Copertina

Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes

Fuente: Wiley Open Access

Salvato in:

Dettagli Bibliografici
Autori principali:	Margriet Johansen, Gloria T. Haskell, Alexandra Arreola, Christine Riordan, Inder K. Gadi, Andrea Penton, Peter R. Papenhausen, Stuart Schwartz
Natura:	Artículo Open Access
Pubblicazione:	Wiley 2024
Soggetti:	Prenatal Diagnosis
Accesso online:	Acceder al recurso
Tags:	Aggiungi Tag Nessun Tag, puoi essere il primo ad aggiungerne!!

Documenti analoghi

A Practical Prenatal Ultrasound Classification System for Lower Limb Anomalies—PRELLIM Classification
di: Arda Arduç, et al.
Pubblicazione: (2025)

The role of confined placental mosaicism in fetal growth restriction: A retrospective cohort study
di: Geerke M. Eggenhuizen, et al.
Pubblicazione: (2024)

Phenotype‐to‐Genotype Description of Prenatal Suspected and Postnatal Discovered Upper Limb Anomalies: A Retrospective Cohort Study
di: Arda Arduç, et al.
Pubblicazione: (2024)

Prenatal Exome Sequencing Analysis in Fetuses With Structural Anomalies: A Multicenter Prospective Cohort Study With Practical Implications
di: Yulin Jiang, et al.
Pubblicazione: (2025)

The Arrival of Exome Sequencing in French Prenatal Diagnosis: An Exploratory Qualitative Study Among Professionals in Prenatal Diagnosis Centers: Prenatome‐SHS
di: Charlène Daval, et al.
Pubblicazione: (2025)

Prenatal Ultrasound in the Diagnosis of Anorectal Malformations: Correlating Prenatal Signs With Postnatal Outcomes
di: D. Huijgen, et al.
Pubblicazione: (2024)

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

Clinical Implications of Noninvasive Prenatal Testing Failures Due to Low Fetal Fraction: Associations With Adverse Maternal and Fetal Outcomes
di: Yuan Ren, et al.
Pubblicazione: (2025)

Analysis of Prenatal Sonographic Features in Rare Fetal Giant Hepatic Hemangioma and Prediction of Prenatal Complications and Prognosis
di: Ling Xu, et al.
Pubblicazione: (2025)

Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis
di: Connor Hartzell, et al.
Pubblicazione: (2025)

High Risk for Rare Autosomal Trisomies Detected by Non‐Invasive Prenatal Testing: Prenatal Diagnosis and Pregnancy Outcomes
di: Zihan Jiang, et al.
Pubblicazione: (2026)

Use of cell‐free non‐invasive prenatal testing in pregnancies affected by placental mosaicism
di: Ida Charlotte Bay Lund, et al.
Pubblicazione: (2024)

Clinical Implications of Low Cell‐Free DNA Fetal Fraction in Non‐Invasive Prenatal Testing: A Retrospective Cohort Study of 40,716 Pregnancies
di: Kayono Yamamoto, et al.
Pubblicazione: (2025)

Hemophilia A: An Ideal Disease for Prenatal Therapy
di: Christopher D. Porada, et al.
Pubblicazione: (2025)

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

Brain Abnormalities in Prenatally Diagnosed Rubinstein‐Taybi Syndrome
di: Laurence S. Carmant, et al.
Pubblicazione: (2025)

Prenatal diagnosis of pontocerebellar hypoplasia with postnatal follow‐up
di: Alienor Jaillard, et al.
Pubblicazione: (2024)

Parental Somatic Mosaicism Detected During Prenatal Diagnosis
di: Natalie J. Chandler, et al.
Pubblicazione: (2024)

Maternal Mosaicism Challenges in Non‐Invasive Prenatal Diagnosis
di: Margot Comel, et al.
Pubblicazione: (2025)

Prenatal Diagnosis of Caroli's Disease by Ultrasound and MRI Imaging
di: Ying‐Li Wei, et al.
Pubblicazione: (2025)

Prenatal Diagnostic Testing for Adult‐Onset Neurodegenerative Disease
di: Maya Rawal, et al.
Pubblicazione: (2025)

PIGO Gene Variants: New Insights Into Prenatal Diagnosis
di: A. Zambiasi, et al.
Pubblicazione: (2025)

Prenatal exome sequencing, a powerful tool for improving the description of prenatal features associated with genetic disorders
di: Christel Thauvin‐Robinet, et al.
Pubblicazione: (2024)

CUL3 ‐Related Neurodevelopmental Disorder: Expanding the Prenatal Phenotype
di: Yoel Gofin, et al.
Pubblicazione: (2026)

Vaginal Delivery in Cases of Prenatally Diagnosed Omphalocele: Feasibility and Outcomes
di: H. Heinrich, et al.
Pubblicazione: (2025)

The Importance of Clinical Acumen for Prenatal Diagnosis in an Increasingly Technological World
di: Teresa N. Sparks, et al.
Pubblicazione: (2025)

Quality of Evidence for Prenatal Down Syndrome Screening: An Umbrella Review
di: Yuehua Zhang, et al.
Pubblicazione: (2026)

Optical Genome Mapping for Prenatal Diagnosis in Fetuses With Structural Anomalies
di: Yiyun Xu, et al.
Pubblicazione: (2025)

Prenatal Ultrasound Observations and Postnatal Manifestations Linked to PIGW Variants
di: Xin Chen, et al.
Pubblicazione: (2025)

Approaching Universal Prenatal Detection of Significant Cardiovascular Malformations in Nevada
di: William N. Evans, et al.
Pubblicazione: (2024)

Prenatal Screening for Fetal X‐Linked Ichthyosis: A Large Cohort Study Combining Non‐Invasive Prenatal Testing and Maternal Serum Unconjugated Estriol Analysis
di: Miao Han, et al.
Pubblicazione: (2026)

Fetal Presentation of MYRF‐Related Cardiac Urogenital Syndrome: An Emerging and Challenging Prenatal Diagnosis
di: Maud Favier, et al.
Pubblicazione: (2024)

Prenatal exome sequencing for the morphologically normal fetus: Should we be doing it?
di: Zhi Gao, et al.
Pubblicazione: (2024)

Prenatal Treatment of Bronchopulmonary Sequestration via Radiofrequency Ablation of the Feeding Artery
di: Hakan Erenel, et al.
Pubblicazione: (2025)

Prenatal Diagnosed Agenesis of the Corpus Callosum: Identifying the Underlying Genetic Etiologies
di: Xing Wei, et al.
Pubblicazione: (2024)

Disparities in Prenatal Carrier Screening Including Partner Testing by Insurance Status
di: Spencer C. Darveau, et al.
Pubblicazione: (2026)

Diagnostic Yield After Postnatal Reanalysis of Prenatal Exome Sequencing Results
di: Kate Swanson, et al.
Pubblicazione: (2025)

Response to the Correspondence by Jean‐Marie Jouannic et al. to: Prenatal Diagnosis and Postnatal Outcome of Closed Spinal Dysraphism. Prenat Diagn. 2024 Apr;44(4):499–510
di: Ivonne Bedei, et al.
Pubblicazione: (2024)

Cytogenetic and Microarray Analysis Follow‐Up of PGT‐A Mosaic and Sex Discrepant Embryos During Pregnancy: Absence of Confirmation and Follow‐Up Recommendations
di: Laura A. Kline, et al.
Pubblicazione: (2026)

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