| |
Article Title |
Author(s) |
Pages |
|
|
|
Cover 1
|
|
OFC
|
|
|
|
Editorial Board
|
|
IFC
|
|
| Review |
| |
Article Title |
Author(s) |
Pages |
|
|
|
The genetics of dyskeratosis congenita
Dyskeratosis congenita (DC) is an inherited bone marrow failure syndrome associated with characteristic mucocutaneous features and a variable series of other somatic abnormalities. The disease is hete...
|
Philip J. Mason,
Monica Bessler
|
635-645
|
|
| Original articles |
| |
Article Title |
Author(s) |
Pages |
|
|
|
Two novel unbalanced whole arm translocations are frequently detected in cervical squamous cell carcinoma
Chromosomal aberrations are a hallmark of human papillomavirus (HPV)-induced cervical carcinogenesis. The aim of this project was to identify structural chromosomal aberrations which may be characteri...
|
Claudia Backsch,
Birgit Pauly,
Melanie Liesenfeld,
Cornelia Scheungraber,
Mieczyslaw Gajda,
Kristin Mrasek,
Thomas Liehr,
Andreas Clad,
Evelin Schrock,
Ingo B. Runnebaum,
Matthias Dürst
et al.
|
646-653
|
|
|
|
Clonal diversity analysis using SNP microarray: a new prognostic tool for chronic lymphocytic leukemia
Chronic lymphocytic leukemia (CLL) is a clinically heterogeneous disease. The methods currently used for monitoring CLL and determining conditions for treatment are limited in their ability to predict...
|
Linsheng Zhang,
Iya Znoyko,
Luciano J. Costa,
Laura K. Conlin,
Robert D. Daber,
Sally E. Self,
Daynna J. Wolff
et al.
|
654-665
|
|
|
|
A t(1;9)(q10;q10) translocation with additional 6q23 and 9q22 rearrangements in a case of chondromyxoid fibroma
Chondromyxoid fibroma (CMF) is a rare cartilaginous tumor of bone. It typically presents in the long tubular bones and to a lesser extent in the small bones of the hands and feet of young adults. To d...
|
Tahereh Dadfarnia,
Gopalrao V.N. Velagaleti,
Kelly D. Carmichael,
Eduardo Eyzaguirre,
Mahmoud A. Eltorky,
Suimin Qiu
et al.
|
666-670
|
|
|
|
Molecular cytogenetic characterization of epithelioid hemangioendothelioma
Epithelioid hemangioendothelioma (EHE) is a rare vascular tumor whose pathological diagnosis can be difficult. In the literature two cases of EHE were found to harbor a balanced t(1;3)(p36.3;q25) tran...
|
Cornelius Woelfel,
Thomas Liehr,
Anja Weise,
Jan Langrehr,
Waleed Amin Kotb,
Manuela Pacyna-Gengelbach,
Detlef Katenkamp,
Iver Petersen
et al.
|
671-676
|
|
| Brief communications |
| |
Article Title |
Author(s) |
Pages |
|
|
|
Similar cytogenetic findings in two synchronous secondary peripheral chondrosarcomas in a patient with multiple osteochondromas
Secondary peripheral chondrosarcoma is a malignant chondroid tumor arising in a benign precursor, either an osteochondroma or an enchondroma. Multiple osteochondromas syndrome (MO) is an autosomal dom...
|
Anastasios I. Kyriazoglou,
Efthimios Dimitriadis,
Niki Arnogiannaki,
Petter Brandal,
Sverre Heim,
Nikos Pandis
et al.
|
677-681
|
|
|
|
Single nucleotide polymorphism array-based karyotyping shows sequential genomic changes from monosomy to copy-neutral loss of heterozygosity of chromosome 7 and 20q deletion within a balanced translocation t(14;20) in AML
Single nucleotide polymorphism array (SNP-A)-based karyotyping can identify copy-neutral loss of heterozygosity (CN-LOH) as well as cryptic lesions not detected by metaphase cytogenetics. We report se...
|
Jungwon Huh,
Yeung Chul Mun,
Chu Myong Seong,
Wha Soon Chung
|
682-686
|
|
|
|
A possible 5′-NRIP1/UHRF1-3′ fusion gene detected by array CGH analysis in a Ph+ ALL patient
A translocation between chromosomes 19 and 21 [dic/t(19;21)(p13;v)] is very rare. To date, only three cases of this particular chromosomal abnormality have been reported. The translocations in these t...
|
Rui Zhang,
Young Mi Kim,
Xiaohe Yang,
Yan Li,
Shibo Li,
Ji-Yun Lee
et al.
|
687-691
|
|
| Letter to the editor |
| |
Article Title |
Author(s) |
Pages |
|
|
|
Sequential transient novel chromosomal translocations in a patient with chronic myelogenous leukemia in complete cytogenetic remission after therapy with imatinib mesylate
Imatinib mesylate (IM) is the first tyrosine kinase inhibitor (TKI) introduced for the treatment of chronic myelogenous leukemia (CML) with remarkable high rates of complete hematologic and cytogeneti...
|
George Papaioannou,
Anastasia Athanasiadou,
Georgia Voutiadou,
Maria Gaitatzi,
Ioannis Batsis,
Tasoula Touloumenidou,
Achilles Anagnostopoulos
et al.
|
692-693
|
|
| Erratum |
| |
Article Title |
Author(s) |
Pages |
|
|
|
Erratum: Long-range massively parallel mate pair sequencing detects distinct mutations and similar patterns of structural mutability in two breast cancer cell lines
Oliver A. Hampton, Maxim Koriabine, Christopher A. Miller, Cristian Coarfa, Jian Li, Petra Den Hollander, Caroline Schoenherr, Lucia Carbone, Mikhail Nefedov, Boudewijn F.H. Ten Hallers, Adrian V. Lee...
|
|
694
|
|
| Frontmatter |
| |
Article Title |
Author(s) |
Pages |
|
|
|
Table of Contents
|
|
A1-A2
|
|
