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skip to content advertisement menu explore journals get published about bmc login my account search search all bmc articles search molecular cytogenetics menu home about articles submission guidelines search submit a manuscript acc 2018 meeting: june 10-13 in snowbird, utah ​​​​​​​ save the date! registration is now open. featured article evaluation of three read-depth based copy number variants (cnv) detection tools using whole-exome sequencing data. articles recent most accessed content type: case report | 20 june 2018 microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disability authors: luca lovrecic, chiara gnan, federica baldan, alessandra franzoni, sara bertok, giuseppe damante, bertrand isidor and borut peterlin content type: obituary | 13 june 2018 yuri b. yurov (1951-2017) authors: ivan y. iourov and svetlana g. vorsanova content type: case report | 13 june 2018 a foetus with 18p11.32-q21.2 duplication and xp22.33-p11.1 deletion derived from a maternal reciprocal translocation t(x;18)(q13;q21.3) authors: jun-kun chen, ping liu, li-qin hu, qing xie, quan-fei huang and hai-liang liu content type: research | 7 june 2018 characterization of chromosome composition of sugarcane in nobilization by using genomic in situ hybridization authors: fan yu, ping wang, xueting li, yongji huang, qinnan wang, ling luo, yanfen jing, xinlong liu, zuhu deng, jiayun wu, yongqing yang, rukai chen, muqing zhang and liangnian xu content type: case report | 7 june 2018 cryptic breakpoint identified by whole-genome mate-pair sequencing in a rare paternally inherited complex chromosomal rearrangement authors: constantia aristidou, athina theodosiou, andria ketoni, mads bak, mana m. mehrjouy, niels tommerup and carolina sismani most recent articles rss view all articles content type: review | 12 october 2011 the genome diversity and karyotype evolution of mammals authors: alexander s graphodatsky, vladimir a trifonov and roscoe stanyon content type: short report | 3 july 2013 intragenic deletion of rbfox1 associated with neurodevelopmental/neuropsychiatric disorders and possibly other clinical presentations authors: wei-wei zhao content type: research | 24 june 2014 diagnostic utility of novel combined arrays for genome-wide simultaneous detection of aneuploidy and uniparental isodisomy in losses of pregnancy authors: stefanie bug, beate solfrank, felizitas schmitz, jana pricelius, mona stecher, andrew craig, marc botcherby and claudia nevinny-stickel-hinzpeter content type: case report | 19 january 2012 marfan syndrome with a complex chromosomal rearrangement including deletion of the fbn1 gene authors: 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 content type: letter | 18 april 2015 comparability of tumor-cytogenetics and -dna-cytometry authors: alfred böcking most accessed articles rss view all articles meetings see here for a list of upcoming genetics meetings . relevant books chromothripsis: methods and protocols pellestor f (editor; 2018) fluorescence in situ hybridization (fish) – application guide liehr t (editor; 2017) 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) editors-in-chief thomas liehr, institute of human genetics, jena, germany henry heng, wayne state university school of medicine, usa founding editor yuri yurov, national research center of mental health, moscow, russia managing editor ivan iourov, national research center of mental health, moscow, russia in memoriam the editors and publisher of molecular cytogenetics regret to announce the death of founding editor yuri yurov. all at the journal wish to express their deepest sadness at his passing and send their condolences to his family and many close friends. an obituary providing an overview of his many scientific accomplishments will be published in the journal shortly. 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. the journal is divided into the following sections: cancer genetics clinical genetics animals and plants mutagenesis nuclear and chromosome architecture technology and methods for more information on the the section aims and scope visit our sections information page . call for papers: chromosomal imbalances and cancer guest editor : emanuela v. volpi, university of westminster chromosomal imbalances have been known as common features of cancer genomes for a long time. however, we have started to comprehend their causative link to tumorigenesis only recently. chromosomal instability – as a process leading to abnormal chromosome content and heterogeneity – has been widely researched and increasingly referred to as driving force behind malignant transformation and defining factor for cancer evolution. the aim of this thematic series is to bring together the latest research findings and conceptual developments in the field of chromosomal imbalances and cancer. we particularly welcome original research papers on the complex interplay of chromosomal instability and aneuploidy in cancerous and pre-cancerous lesions, and papers exploring potential translational aspects. about the european cytogeneticists association the european cytogeneticists association (e.c.a.) was founded in 1997 and is registered in france. the objectives of the association are: representation and promotion of fundamental research and applications of cytogenetics organisation, assessment, and quality control of cytogenetic services in europe research, education and training in all fields which are of interest to or concern cytogenetics and cytogeneticists facilitation of transfer of information and collaboration between laboratories. representation of professionals in cytogenetics study of questions and defence of interests concerning cytogeneticists or cytogenetics in general visit the e.c.a website to find out more. advertisement submit a manuscript editorial board sign up for article alerts and news from this journal official journal of learn more about the society here. follow follow us on twitter 2016 journal metrics speed 24 days from submission to first decision 11 days from acceptance to publication citation impact 1.455 - 2-year impact factor 1.558 - 5-year impact factor 0.612 - source normalized impact per paper (snip) 0.616 - scimago journal rank (sjr) usage 232,199 downloads 814 usage factor social media impact 57 mentions more about our metrics advertisement molecular cytogenetics issn: 1755-8166 contact us submission enquiries: [email protected] general enquiries: [email protected] explore journals get published about bmc read more on our blogs receive bmc newsletters manage article alerts language editing for authors scientific editing for authors policies accessibility press center contact us leave feedback careers follow bmc bmc twitter page bmc facebook page bmc google plus page bmc weibo page by using this website, you agree to our terms and conditions , privacy statement and cookies policy. manage the cookies we use in the preference centre. © 2018 biomed central ltd unless otherwise stated. part of springer nature .