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Retricted access

Research article

First published 2015-3

An Additional Patient With 3q27.3 Microdeletion Syndrome

Marco Castori, Irene Bottillo, Luigi Laino [...]

Journal of Child Neurology

Open access

Research article

First published 2022-7

Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of chromosome 16p11.2

Meihua Li, Linlin Liu, Yijun Wu [...]

Journal of International Medical Research

Open access

Research article

First published 2018-1

Molecular microdeletion analysis of infertile men with karyotypic Y chromosome abnormalities

Yuan Pan, Hong-guo Zhang, QI Xi [...]

Journal of International Medical Research

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Case report

First published 2018-7

Cleidocranial Dysplasia with 6p21.1-p12.3 Microdeletion

Surasak Puvabanditsin, Melissa February, Julia Mayne [...]

The Cleft Palate Craniofacial Journal

Open access

Research article

First published 2020

Optimising immunisation in children with 22q11 microdeletion

Angela Berkhout, Kahn Preece, Vanil Varghese [...]

Therapeutic Advances in Vaccines and Immunotherapy

Open access

Research article

First published 2020-4

Chromosomal abnormalities and Y chromosome microdeletions in infertile men with azoospermia and oligozoospermia in Eastern China

Jing Sha, Guiping Huang, Bei Zhang [...]

Journal of International Medical Research

Free access

Research article

First published 2012-5

Microdeletion and Microduplication Syndromes

Anja Weise, Kristin Mrasek, Elisabeth Klein [...]

Journal of Histochemistry & Cytochemistry

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Research article

First published 2015-1

16p13.11 Microdeletion in a Patient With Hemiconvulsion-Hemiplegia-Epilepsy Syndrome

Christina I. Miteff, Robert L. Smith, Nicole L. Bain [...]

Journal of Child Neurology

Free access

Research article

First published 2012-2

A New Molecular Diagnostic Approach to Assess Y Chromosome Microdeletions in Infertile Men

K Sun, X-F Chen, X-B Zhu [...]

Journal of International Medical Research

Open access

Case report

First published 2022-9

Prenatal diagnosis and molecular cytogenetic characterization of an inherited microdeletion of 18q12.3 encompassing SETBP1

Yaqing Zhou, Yan Quan, Yijun Wu [...]

Journal of International Medical Research

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