Sage Journals: Discover world-class research

Retricted access

Research article

First published 2023-5

Aortic Arch Laterality in Chromosome 22q11.2 Deletion Syndrome: Male-Female Difference

William N. Evans, Ruben J. Acherman, Humberto Restrepo

Clinical Pediatrics

Retricted access

Research article

First published 2004-4

Association of Anterior Glottic Webs with Velocardiofacial Syndrome (Chromosome 22q11.2 Deletion)

R. Christopher Miyamoto, Robin T. Cotton, Alan F. Rope [...]

Otolaryngology–Head and Neck Surgery

Retricted access

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

Retricted access

Other

First published 2004-05

Frontal and Caudate Alterations in Velocardiofacial Syndrome (Deletion at Chromosome 22q11.2)

Wendy R. Kates, Courtney P. Burnette, Brandy A. Bessette [...]

Journal of Child Neurology

Retricted access

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

Retricted access

Case report

First published 2019-1

22q11.2 Deletion Syndrome in Colombian Patients With Syndromic Cleft Lip and/or Palate

Suleima Carpeta, Tatiana Pineda, Maria Claudia Martínez [...]

The Cleft Palate Craniofacial Journal

Retricted access

Case report

First published 2016-6-22

Severe laryngeal stenosis in newly born twins with 22q11.2 deletion syndrome: A case report

B. Clive, G. Corsten, L.S. Penney [...]

Journal of Neonatal-Perinatal Medicine

Retricted access

Research article

First published 1997-1

PCR Assay for Screening Patients At Risk for 22q11.2 Deletion

Deborah A. Driscoll, Beverly S. Emanuel, Laura E. Mitchell [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Research article

First published 2006-7

Evaluation of Potential Modifiers of the Palatal Phenotype in the 22q11.2 Deletion Syndrome

Deborah A. Driscoll, Torrey Boland, Beverly S. Emanuel [...]

The Cleft Palate Craniofacial Journal

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

Search results