Cover Image

The “Dynamic Tongue Contraction Technique” for Diagnosis of Soft Palate Cleft in Cases of Cleft Lip and Palate Sequence

Fuente: Wiley Open Access

Saved in:

Bibliographic Details
Main Authors:	Ettie Piura, Yoav Alpert, Or Touval, Offra Engel, Biader Samih Bilal, Yaniv Ebner, Ofer Markovitch
Format:	Artículo Open Access
Published:	Wiley 2026
Subjects:	Prenatal Diagnosis
Online Access:	Acceder al recurso
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Prenatal Diagnosis of Sotos Syndrome: Integrating Chromosomal Microarray Analysis and Exome Sequencing
by: Xi Yang, et al.
Published: (2025)

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

Diagnostic Yield of Sequencing for Prenatal Diagnosis of Fetal Structural Anomalies: An Updated Systematic Review
by: Karen Mei Xian Lim, et al.
Published: (2026)

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

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

Fetal Sequencing: Lessons Learnt and Challenges Remaining
by: Lyn S. Chitty
Published: (2026)

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

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

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

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

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

Navigating the Challenges of Exome Sequencing in Structurally Normal Fetuses
by: Sylvie Langlois, et al.
Published: (2025)

The Challenges of Performing Exome Sequencing in Structurally Normal Fetuses
by: Natalie Chandler, et al.
Published: (2024)

Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia
by: Yan Lü, et al.
Published: (2024)

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

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

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

Diagnostic Yield of Exome Sequencing for Pregnancies With and Without Fetal Anomalies and for Stillbirth
by: Roni Zemet, et al.
Published: (2025)

Global Delivery of Foetal Sequencing: Do We Need Some Standardisation?
by: Natalie J. Chandler, et al.
Published: (2025)

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

Prenatal Diagnosis of Horseshoe Lung: A Report of Three Cases and Review of the Literature
by: Benjamin Birene, et al.
Published: (2025)

Perspectives on Fetal Sex and Prenatal Diagnosis of Differences of Sex Development Among Midwives
by: Madeline Dingle, et al.
Published: (2025)

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

Aberrant Fetal Brain Sulcus Formation: A Clue to the Diagnosis of Sotos Syndrome
by: Caiqun Luo, et al.
Published: (2024)

Congenital Vascular Anomalies: Prenatal Diagnosis, Perinatal Outcome and Postnatal Follow up
by: Stefano Faiola, et al.
Published: (2025)

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

Novel Missense Variant in the FGFR1 Gene Associated With Prenatal Diagnosis of Hartsfield Syndrome
by: Mia B. Hodges, et al.
Published: (2025)

Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder
by: Xiang‐Yi Jing, et al.
Published: (2025)

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

Prenatal Diagnosis of Myhre Syndrome in Two Cases: Further Delineation of the Cardiac and External Phenotype
by: Jeanne Jury, et al.
Published: (2024)

Neurocognitive Assessment in Children With Prenatal Diagnosis of Apparently Isolated Obliteration of Cavum Septi Pellucidi
by: Elisa Montaguti, et al.
Published: (2025)

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

Clinical and Molecular Features of Ciliopathies Diagnosed by Prenatal Exome Sequencing in Fetuses With Ultrasound Abnormalities
by: Xiaofan Zhu, et al.
Published: (2025)

The Value of Enhancing Sonographic Phenotyping to Improve the Diagnostic Yield of Noninvasive Prenatal Diagnosis (NIPD) for Achondroplasia
by: Camille Verebi, et al.
Published: (2025)

Prenatal Diagnosis of Congenital Paraesophageal Hernia With Gastric Volvulus and Postnatal FBN1 Mutation Confirmation
by: Spencer C. Darveau, et al.
Published: (2025)

Celocentesis for Prenatal Diagnosis of Rare Monogenic Diseases: Development, Validation, and Clinical Outcome on 876 Cases
by: Antonino Giambona, et al.
Published: (2026)

Prenatal Diagnosis of Congenital Heart Disease in a Developing Country—A Cross‐Sectional Study
by: Lina Hammoud, et al.
Published: (2026)

Perinatal Survival Following Parvovirus B19 Infection: Overall Outcomes and a Secondary Comparison of the 2023–2024 Outbreak to the Previous Two Decades
by: Noam Regev, et al.
Published: (2025)

Exome Sequencing in Prenatally Diagnosed Isolated Neural Tube Defects: A Subtype‐Specific Analysis
by: Adi Botvinik, et al.
Published: (2026)

Exome Sequencing of Fetuses With Intracranial Hemorrhage Unravels Novel Causative Genes and an Extreme Genetic Heterogeneity
by: Thibault Coste, et al.
Published: (2025)