Molecular Cytogenetics

Molecular Cytogenetics encompasses all aspects of chromosome biology and the application of molecular cytogenetic techniques in all areas of biomedicine, including structural and functional organization of the chromosome and nucleus, genome variation, expression and evolution, chromosome abnormalities and genomic variations in medical genetics and tumor genetics.

Editors-in-Chief

Thomas Liehr, Institute of Human Genetics, Jena, Germany
Henry Heng, Wayne State University School of Medicine, USA
Yuri Yurov, National Research Center of Mental Health, Moscow, Russia

Managing and Section Editor - medical genetics

Ivan Iourov, National Research Center of Mental Health, Moscow, Russia

Section Editor - tumorgenetics

Aurelia Meloni-Ehrig, Ameripath

Editorial Board | Instructions for authors | FAQ

Articles

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Research

Genetic testing for hearing loss in the United States should include deletion/duplication analysis for the deafness/infertility locus at 15q15.3

Hoppman N, Aypar U, Brodersen P, Brown N, Wilson J and Babovic-Vuksanovic D Molecular Cytogenetics 2013, 6:19 (6 May 2013)
Case report

A de novo acute myeloid leukemia (AML-M4) case with a complex karyotype and yet unreported breakpoints

Al-achkar W, Aljapawe A, Othman MA and Wafa A Molecular Cytogenetics 2013, 6:18 (5 May 2013)
Research

Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature review

Hemmat M, Hemmat O, Anguiano A, Boyar FZ, El Naggar M, Wang JC, Wang BT, Sahoo T et al. Molecular Cytogenetics 2013, 6:17 (2 May 2013)
Reviewer Acknowledgement

Reviewer acknowledgement 2013

Liehr T, Heng H and Yurov Y Molecular Cytogenetics 2013, 6:9 (15 April 2013)
Short report

Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years’ clinical application for over 8,700 patients

Ahn JW, Bint S, Bergbaum A, Mann K, Hall RP and Ogilvie CM Molecular Cytogenetics 2013, 6:16 (5 April 2013)
Case report

De novo triplication of 11q12.3 in a patient with developmental delay and distinctive facial features

Yamamoto T, Matsuo M, Shimada S, Sangu N, Shimojima K, Aso S and Saito K Molecular Cytogenetics 2013, 6:15 (3 April 2013)
Research

Heteromorphic variants of chromosome 9

Kosyakova N, Grigorian A, Liehr T, Manvelyan M, Simonyan I, Mkrtchyan H, Aroutiounian R, Polityko AD et al. Molecular Cytogenetics 2013, 6:14 (1 April 2013)
Research

Cytogenetic analysis in three Bryconamericus species (Characiformes, Characidae): first description of the 5S rDNA-bearing chromosome pairs in the genus

Piscor D, Ribacinko-Piscor DB, Fernandes CA and Parise-Maltempi PP Molecular Cytogenetics 2013, 6:13 (1 April 2013)
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Comments

Complex translocation versus independent abnormalities in...

Comment on: Yokota et al. Molecular Cytogenetics 2012, 5:20
Correction of proband's karyotype.

Comment on: Manolakos et al. Molecular Cytogenetics 2011, 4:6
Correction to typographical error

Comment on: Manolakos et al. Molecular Cytogenetics 2010, 2:26

Indexing news

Molecular Cytogenetics is now being tracked by Thomson Reuters (ISI). We hope to receive our first official impact factor in 2013. Keep checking the website for further updates.

Latest review

The utility of copy number variation (CNV) in studies of hypertension-related left ventricular hypertrophy (LVH): rationale, potential and challenges

BoonPeng H and Yusoff K

Molecular Cytogenetics 2013, 6:8

Meetings

List of genetic meetings

Publish the genome in 3D!

Reconstruction of chromosome 19 in a central position in a human sperm cell, offers new insight into positional effects. Molecular Cytogenetics offers unlimited space for figures and movies, embedded in articles.