Front & Back Matter

Abstract

203 48th European Mathematical Genetics Meeting (EMGM) 2020 Lausanne, Switzerland, April 16–17, 2020 Guest Editors: Zoltan Kutalik; Matthew Robinson (Lausanne) Cover illustration iStock.com Cytogenetic and Genome Research has been the leading forum for original reports and reviews in human and animal cytogenetics, including molecular, clinical and comparative cytogenetics. In recent years, most of the contributions have centered on genome research, including gene regulation and expression, cancer genetics, comparative genetics and human malformation syndromes. The journal publishes key papers on the insights into the mechanisms of chromosome aberrations in somatic, meiotic and malignant cells. Its scope includes studies on invertebrate and plant cytogenetics and genomics. Also featured are recent international reports on human and animal chromosome nomenclature. In addition to regular issues, the journal has been publishing since 2002 a series of topical issues on a broad variety of themes from cytogenetic and genome research. Cytogenetic and Genome Research Founded: 1962 Category: Basic Research Field of Interest: Genetics Listed in bibliographic services, including: PubMed/MEDLINE, Web of Science, Google Scholar, Scopus, Embase 2019: Volumes 157, 158, 159 4 issues per volume Language: English ISSN 1424–8581 e-ISSN 1424–859X More information at w w w.karger.com/cgr A leading journal on human, animal and plant genomes and chromosomes Impact Factor: 1.587 5-Year Impact Factor: 1.682 Editor-in-Chief M. Schmid, Würzburg Executive Editors L.A. Cannizzaro, New York, NY T. Haaf, Würzburg Managing Editors T. Gößwein, Würzburg M. Guttenbach, Würzburg K. Schmid, Würzburg Associate Editors R.D. Burnside, Research Triangle Park, NC A. Geurts Van Kessel, Nijmegen A. Houben, Gatersleben O. Riess, Tübingen J. Smith, Roslin Selected contributions • Two Cases with Ring Chromosome 13 at either End of the Phenotypic Spectrum: Çakmaklı, S.; Çankaya, T.; Gürsoy, S.; Koç, A.; Kırbıyık, Ö.; Kılıçarslan, Ö.A.; Özer, E.; Erçal, D.; Bozkaya, Ö.G. (Izmir) • Clinical, Hormonal, and Genetic Evaluation of Idiopathic Nonobstructive Azoospermia and Klinefelter Syndrome Patients: Kim, S.Y.; Lee, B.Y.; Oh, A.R.; Park, S.Y.; Lee, H.S.; Seo, J.T. (Seoul) • Prenatal Diagnosis of Trisomy 2p due to Terminal 2p Duplication including Interstitial Telomeric Sequences: Marlet, L.; Alix, E.; Till, M. (Bron); Raskin-Champion, F.; Attia, J.; Boggio, D. (Pierre-Bénite); Sanlaville, D.; Schluth-Bolard, C. (Bron) • The Relationship between the (In-)Stability of NORs and Their Chromosomal Location: The Example of Cercopithecidae and a Short Review of Other Primates: Gerbault-Seureau, M.; Cacheux, L.; Dutrillaux, B. (Paris) • Production and Molecular Cytogenetic Characterization of a Durum Wheat-Thinopyrum elongatum 7E Disomic Addition Line with Resistance to Fusarium Head Blight: Liu, H.; Dai, Y. (Yangzhou/Ottawa, ON); Chi, D. (Ottawa, ON); Huang, S. (Nanjing); Li, H.; Duan, Y. (Yangzhou); Cao, W. (Ottawa, ON); Gao, Y. (Yangzhou); Fedak, G. (Ottawa, ON); Chen, J. (Yangzhou) • Human Malformation Syndromes of Defective GLI: Opposite Phenotypes of 2q14.2 (GLI2) and 7p14.2 (GLI3) Microdeletions and a GLIA/R Balance Model: Niida, Y. (Uchinada); Inoue, M. (Kanazawa); Ozaki, M.; Takase, E. (Uchinada) • Familial Duplication/Deletion of 1q42.13q43 as Meiotic Consequence of an Intrachromosomal Insertion in Chromosome 1: Silipigni, R.; Monfrini, E.; Baccarin, M.; Giangiobbe, S.; Lalatta, F.; Guerneri, S.; Bedeschi, M.F. (Milan)