Sage Journals: Discover world-class research

Retricted access

Research article

First published 2016-11

Vascular Ring Diagnosis and Management

William N. Evans, Ruben J. Acherman, Michael L. Ciccolo [...]

World Journal for Pediatric and Congenital Heart Surgery

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Review article

First published 1997-05

Chromosome 22q1l Deletion Syndrome: An Update and Review for the Primary Pediatrician

Janet A. Thomas, John M. Graham

Clinical Pediatrics

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Research article

First published 2001-11

Pulmonary Arterial Aneurysm with CATCH 22 Syndrome

Osamu Kinoshita, Tetsuro Mizoue, Akitoshi Kusama [...]

Angiology

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Other

First published 1976-07

The Problem of Trisomy 22

Hans Zellweger, Victor Ionasescu, Jane Simpson [...]

Clinical Pediatrics

Open access

Case report

First published 2016-4

Specific behavioural phenotype and secondary cognitive decline as a result of an 8.6 Mb deletion of 2q32.2q33.1

Hojka Gregoric Kumperscak, Danijela Krgovic, Nadja Kokalj Vokac

Journal of International Medical Research

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Research article

First published 2001-11

Choroid Plexus Carcinomas and Rhabdoid Tumors: Phenotypic and Genotypic Overlap

Josephine Wyatt-Ashmead, Bette Kleinschmidt-DeMasters, Gary W. Mierau [...]

Pediatric and Developmental Pathology

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Other

First published 2001-06

Three New Patients With Congenital Unilateral Facial Nerve Palsy due to Chromosome 22q11 Deletion

Jesús Eirís Puñal, Manuel Fuster Siebert, Francisco Barros Angueira [...]

Journal of Child Neurology

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Research article

First published 2004-06

GJB2 and GJB6 Mutations in 165 Danish Patients Showing Non-Syndromic Hearing Impairment

Karen Gr⊘nskov, Lars Allan Larsen, Nanna Dahl Rendtorff [...]

Genetic Testing and Molecular Biomarkers

Free access

Research article

First published 2017-1

Elevation of plasma-soluble HLA-G in childhood nephrotic syndrome is associated with IgE

Yanqing Liu, Meimei Lai, Yunyan Lou [...]

Annals of Clinical Biochemistry: International Journal of Laboratory Medicine

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Brief report

First published 2003-12

Multiplex Ligation-Dependent Probe Amplification (MLPA) Detects Large Deletions in the MECP2 Gene of Swedish Rett Syndrome Patients

Anna Erlandson, Lena Samuelsson, Bengt Hagberg [...]

Genetic Testing and Molecular Biomarkers

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