Skip to main content Advertisement Menu Search Search Publisher main menu Journals Submissions Publishing services About My Account Follow BioMed Central Twitter Facebook Molecular Cytogenetics Molecular Cytogenetics main menu Home About Articles Featured review: Cytogenetically visible copy number variations Read More Articles Recent Most accessed Recent articles Recent articles RSS 1. Short report Primary and recurrent diffuse astrocytomas: genomic profile comparison reveals acquisition of biologically relevant aberrations Halka Lhotska, Zuzana Zemanova, Hana Cechova, Sarka Ransdorfova, Karla Svobodova, Filip Kramar, Zdenek Krejcik and Kyra Michalova Published on: 9 February 2016 2. Hypothesis The paradox of longer sperm telomeres in older men’s testes: a birthcohort effect caused by transgenerational telomere erosion in the female germline Reinhard Stindl Published on: 8 February 2016 3. Case Report Proximal 21q deletion as a result of a de novo unbalanced t(12;21) translocation in a patient with dysmorphic features, hepatomegaly, thick myocardium and delayed psychomotor development Cathrine Jespersgaard, Ida N. Damgaard, Nanna Cornelius, Iben Bache, Niels Knabe, Maria J. Miranda and Zeynep Tümer Published on: 4 February 2016 4. Research CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes Emanuele G. Coci, Udo Koehler, Thomas Liehr, Armin Stelzner, Christian Fink, Hendrik Langen and Joachim Riedel Published on: 3 February 2016 5. Research Preferential Y-Y pairing and synapsis and abnormal meiotic recombination in a 47,XYY man with non obstructive azoospermia Caiyun Wu, Liu Wang, Furhan Iqbal, Xiaohua Jiang, Ihtisham Bukhari, Tonghang Guo, Gengxin Yin, Howard J. Cooke, Zhenyi Cao, Hong Jiang and Qinghua Shi Published on: 2 February 2016 View all articles Most accessed articles Most accessed articles RSS 1. Research Diagnostic utility of novel combined arrays for genome-wide simultaneous detection of aneuploidy and uniparental isodisomy in losses of pregnancy Stefanie Bug, Beate Solfrank, Felizitas Schmitz, Jana Pricelius, Mona Stecher, Andrew Craig, Marc Botcherby and Claudia Nevinny-Stickel-Hinzpeter Published on: 24 June 2014 2. Short report Intragenic deletion of RBFOX1 associated with neurodevelopmental/neuropsychiatric disorders and possibly other clinical presentations Wei-Wei Zhao Published on: 3 July 2013 3. Review The genome diversity and karyotype evolution of mammals Alexander S Graphodatsky, Vladimir A Trifonov and Roscoe Stanyon Published on: 12 October 2011 4. Letter Comparability of tumor-cytogenetics and -DNA-cytometry Alfred Böcking Published on: 18 April 2015 5. Case report Marfan syndrome with a complex chromosomal rearrangement including deletion of the FBN1 gene Mileny ES Colovati, Luciana RJ da Silva, Sylvia S Takeno, Tatiane I Mancini, Ana R N Dutra, Roberta S Guilherme, Cláudia B de Mello, Maria I Melaragno and Ana B A Perez Published on: 19 January 2012 View all articles 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 Editor Ivan Iourov, National Research Center of Mental Health, Moscow, Russia Aims and scope Molecular Cytogenetics encompasses all aspects of chromosome biology and the application of molecular cytogenetic techniques in all areas of biology and medicine, 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. Meetings See here for a list of upcoming genetics meetings. Relevant books Uniparental Disomy (UPD) in Clinical Genetics Liehr T (2014) Human Interphase Chromosomes Yurov YB, Vorsanova SG, Iourov IY (2013) Small Supernumerary Marker Chromosomes (sSMC) Liehr T (2012) Fluorescence In Situ Hybridization (FISH) - Application Guide Liehr T (2009) FISH Technology Rautenstrauss BW, Liehr T (2002) Submit a manuscript Submission Guidelines Editorial Board Sign up to article alerts Impact Factor: 2.140 Follow Follow us on Twitter ISSN: 1755-8166 Advertisement Contact us Jobs Manage manuscripts Sign up for article alerts Manage article alerts Leave feedback Press center Read more on our blogs Policies Licensing Terms and conditions Privacy statement Accessibility Cookies Follow BioMed Central Twitter Facebook Google Plus YouTube LinkedIn Reddit Weibo © 2016 BioMed Central Ltd unless otherwise stated. Part of Springer Science+Business Media. By continuing to use this website, you agree to our Terms and Conditions, Privacy statement and Cookies policy.