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Cytogenetic and Genome Research

Vol. 145, No. 1, 2015

Issue release date: June 2015

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Case Report
1

A Novel 23.1 Mb Interstitial Deletion Involving 7q22.3q32.1 in a Girl with Short Stature, Motor Delay, and Craniofacial Dysmorphism

del Refugio Rivera-Vega M. · Gómez-del Angel L.A. · Valdes-Miranda J.M. · Pérez-Cabrera A. · Gonzalez-Huerta L.M. · Toral-López J. · Cuevas-Covarrubias S.
Cytogenet Genome Res 2015;145:1-5 (DOI:10.1159/000381234)
6

35-Year Follow-Up of a Case of Ring Chromosome 2: Array-CGH Analysis and Literature Review of the Ring Syndrome

Sarri C. · Douzgou S. · Kontos H. · Anagnostopoulou K. · Tümer Z. · Grigoriadou M. · Petersen M.B. · Kokotas H. · Merou K. · Pandelia E. · Giouroukou E. · Papanikolaou K. · Côté G.B. · Gyftodimou Y.
Cytogenet Genome Res 2015;145:6-13 (DOI:10.1159/000382046)
14

Molecular Delineation of Partial Trisomy 14q and Partial Trisomy 12p in a Patient with Dysmorphic Features, Heart Defect and Developmental Delay

Bose D. · Krishnamurthy V. · Venkatesh K.S. · Aiyaz M. · Shetty M. · Rao S.N. · Kutty A.V.M.
Cytogenet Genome Res 2015;145:14-18 (DOI:10.1159/000381294)
19

Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay

Papoulidis I. · Paspaliaris V. · Papageorgiou E. · Siomou E. · Dagklis T. · Sotiriou S. · Thomaidis L. · Manolakos E.
Cytogenet Genome Res 2015;145:19-24 (DOI:10.1159/000381568)
25

Co-Occurence of Reciprocal Translocation and COL2A1 Mutation in a Fetus with Severe Skeletal Dysplasia: Implications for Genetic Counseling

Heinrich T. · Nanda I. · Rehn M. · Zollner U. · Ernestus K. · Wirth C. · Schlüter G. · Schmid M. · Kunstmann E.
Cytogenet Genome Res 2015;145:25-28 (DOI:10.1159/000381169)
Original Article
29

Distal Partial Trisomy 15q26 and Partial Monosomy 16p13.3 in a 36-Year-Old Male with Clinical Features of Both Chromosomal Abnormalities

Cox D.M. · Butler M.G.
Cytogenet Genome Res 2015;145:29-34 (DOI:10.1159/000381293)
35

Asynchronous Replication in Lymphocytes from Patients with Inflammatory Bowel Disease and Primary Sclerosing Cholangitis

Laish I. · Biron-Shental T. · Katz H. · Liberman M. · Kitay-Cohen Y. · Konikoff F.M. · Amiel A.
Cytogenet Genome Res 2015;145:35-41 (DOI:10.1159/000381406)
42

Comprehensive Analyses of White-Handed Gibbon Chromosomes Enables Access to 92 Evolutionary Conserved Breakpoints Compared to the Human Genome

Weise A. · Kosyakova N. · Voigt M. · Aust N. · Mrasek K. · Löhmer S. · Rubtsov N. · Karamysheva T.V. · Trifonov V.A. · Hardekopf D. · Jančušková T. · Pekova S. · Wilhelm K. · Liehr T. · Fan X.
Cytogenet Genome Res 2015;145:42-49 (DOI:10.1159/000381764)
Editor's Choice - Free Access
50

Bisphenol A Exposure during Oocyte Maturation in vitro Results in Spindle Abnormalities and Chromosome Misalignment in Bos taurus

Ferris J. · Favetta L.A. · King W.A.
Cytogenet Genome Res 2015;145:50-58 (DOI:10.1159/000381321)
59

A High-Resolution Comparative Chromosome Map of Cricetus cricetus and Peromyscus eremicus Reveals the Involvement of Constitutive Heterochromatin in Breakpoint Regions

Vieira-da-Silva A. · Louzada S. · Adega F. · Chaves R.
Cytogenet Genome Res 2015;145:59-67 (DOI:10.1159/000381840)
68

Molecular and Cytological Comparisons of Chromosomes 7el1, 7el2, 7Ee, and 7Ei Derived from Thinopyrum

Guo J. · He F. · Cai J.-J. · Wang H.-W. · Li A.-F. · Wang H.-G. · Kong L.-R.
Cytogenet Genome Res 2015;145:68-74 (DOI:10.1159/000381838)