Sage Journals: Discover world-class research

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Research article

First published 2001-5

Congenital cardiac malformations in fetuses with chromosome 22q11.2 microdeletion (CATCH 22)

Cornelia Tennstedt, Petra Zschieschang, Rabih Chaoui [...]

Electronic Journal of Pathology and Histology

Free access

Research article

First published 2025-3

Real-World Treatment of Schizophrenia in Adults With a 22q11.2 Microdeletion: Traitement dans le monde réel de la schizophrénie chez des adultes atteints du syndrome de microdélétion 22q11.2

Lily Van, Tracy Heung, Nikolai Gil D. Reyes [...]

The Canadian Journal of Psychiatry

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Research article

First published 2007-1

Clinical Correlation of Chromosome 22q11.2 Fluorescent in Situ Hybridization Analysis and Velocardiofacial Syndrome

Albert K. Oh, Laura A. Workman, Granger B. Wong

The Cleft Palate Craniofacial Journal

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Research article

First published 2004-1

Unusual Phenotypes Associated with Microdeletion 22Q11.2

L. Florez, P. Rojas, D. Moscatello [...]

Journal of Investigative Medicine

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Research article

First published 2015-4

Mosaic 22q11.2 Deletion and Tetralogy of Fallot With Absent Pulmonary Valve

Sudesh Prabhu, Bryan Jenny, Harraway James [...]

World Journal for Pediatric and Congenital Heart Surgery

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Brief report

First published 2024-7

Short Report: Clinical Features and Epilepsy Monitoring in an Adult With 22q11.2 Deletion Syndrome

Mike W. Zhang, Stephanie T. Bustros, Tyler E. Gaston [...]

The Neurohospitalist

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Other

First published 2005-01

Neurogenic Arthrogryposis Multiplex Congenita and Velopharyngeal Incompetence Associated With Chromosome 22q11.2 Deletion

Manuel Castro-Gago, José María Iglesias-Meleiro, Manuel Oscar Blanco-Barca [...]

Journal of Child Neurology

Open access

Research article

First published 2025-9

Frequency of Genetic Abnormalities in Cases of Conotruncal Anomalies—A Single-center Prospective Observational Study

Radhika Uppal, Nitin Rao, Suman Vyas [...]

Indian Journal of Clinical Cardiology

Open access

Research article

First published 2021

CNVs in the 22q11.2 Chromosomal Region Should Be an Early Suspect in Infants with Congenital Cardiac Disease

Tatiana Pineda, Ignacio Zarante, Angela Camila Paredes [...]

Clinical Medicine Insights: Cardiology

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Research article

First published 2018-6

Airway Anomalies in Patients With 22q11.2 Deletion Syndrome: A 5-Year Review

Joel W. Jones, Meghan Tracy, Mollie Perryman [...]

Annals of Otology,Rhinology & Laryngology

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