Additional file 1 - Molecular Cytogenetics

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Molecular Cytogenetics
Molecular Cytogenetics main menu
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Articles
Featured review: Cytogenetically visible copy number
variations
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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
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Most accessed articles
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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)
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ISSN:
1755-8166
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