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Vol. 135, No. 3-4, 2011

Issue release date: December 2011

The Genome-Wide Array Revolution in Clinical Cytogenetics: From Discoveries to Diagnoses

See also ISBN 978-3-8055-9939-9 for more details
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Title Page / Table of Contents

Cytogenet Genome Res 2011;135:167–170 (DOI:10.1159/000335013)
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Poot M.
Cytogenet Genome Res 2011;135:171–173 (DOI:10.1159/000334062)

Genome Arrays for the Detection of Copy Number Variations in Idiopathic Mental Retardation, Idiopathic Generalized Epilepsy and Neuropsychiatric Disorders: Lessons for Diagnostic Workflow and Research

Hochstenbach R. · Buizer-Voskamp J.E. · Vorstman J.A.S. · Ophoff R.A.
Cytogenet Genome Res 2011;135:174–202 (DOI:10.1159/000332928)

Clinical Laboratory Implementation of Cytogenomic Microarrays

South S.T. · Brothman A.R.
Cytogenet Genome Res 2011;135:203–211 (DOI:10.1159/000331425)

SNP Array Analysis in Constitutional and Cancer Genome Diagnostics – Copy Number Variants, Genotyping and Quality Control

de Leeuw N. · Hehir-Kwa J.Y. · Simons A. · Geurts van Kessel A. · Smeets D.F. · Faas B.H.W. · Pfundt R.
Cytogenet Genome Res 2011;135:212–221 (DOI:10.1159/000331273)

Interpretation of Array Comparative Genome Hybridization Data: A Major Challenge

Gijsbers A.C.J. · Schoumans J. · Ruivenkamp C.A.L.
Cytogenet Genome Res 2011;135:222–227 (DOI:10.1159/000334066)

Disentangling the Myriad Genomics of Complex Disorders, Specifically Focusing on Autism, Epilepsy, and Schizophrenia

Poot M. · van der Smagt J.J. · Brilstra E.H. · Bourgeron T.
Cytogenet Genome Res 2011;135:228–240 (DOI:10.1159/000334064)

From Karyotyping to Array-CGH in Prenatal Diagnosis

Lichtenbelt K.D. · Knoers N.V.A.M. · Schuring-Blom G.H.
Cytogenet Genome Res 2011;135:241–250 (DOI:10.1159/000334065)

Challenges of Interpreting Copy Number Variation in Syndromic and Non-Syndromic Congenital Heart Defects

Breckpot J. · Thienpont B. · Arens Y. · Tranchevent L.C. · Vermeesch J.R. · Moreau Y. · Gewillig M. · Devriendt K.
Cytogenet Genome Res 2011;135:251–259 (DOI:10.1159/000331272)

Array CGH in Human Leukemia: From Somatics to Genetics

van der Veken L.T. · Buijs A.
Cytogenet Genome Res 2011;135:260–270 (DOI:10.1159/000330629)

Origins and Breakpoint Analyses of Copy Number Variations: Up Close and Personal

van Binsbergen E.
Cytogenet Genome Res 2011;135:271–276 (DOI:10.1159/000330267)

Functional Enrichment Analysis with Structural Variants: Pitfalls and Strategies

Webber C.
Cytogenet Genome Res 2011;135:277–285 (DOI:10.1159/000331670)
Further Section

Author Index Vol. 135, No. 3–4, 2011

Cytogenet Genome Res 2011;135:286 (DOI:10.1159/000335011)
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Contents Vol. 135, 2011

Cytogenet Genome Res 2011;135:I–IV (DOI:10.1159/000333852)
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