Related references
Note: Only part of the references are listed.Genomic and functional variation of human centromeres
Lori L. Sullivan et al.
EXPERIMENTAL CELL RESEARCH (2020)
Methods for mapping 3D chromosome architecture
Rieke Kempfer et al.
NATURE REVIEWS GENETICS (2020)
Refining the Phenotype of Recurrent Rearrangements of Chromosome 16
Serena Redaelli et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2019)
Alpha satellite DNA biology: finding function in the recesses of the genome
Shannon M. McNulty et al.
CHROMOSOME RESEARCH (2018)
The dark side of centromeres: types, causes and consequences of structural abnormalities implicating centromeric DNA
V. Barra et al.
NATURE COMMUNICATIONS (2018)
Nucleolus association of chromosomal domains is largely maintained in cellular senescence despite massive nuclear reorganisation
Stefan Dillinger et al.
PLOS ONE (2017)
Mechanisms underlying structural variant formation in genomic disorders
Claudia M. B. Carvalho et al.
NATURE REVIEWS GENETICS (2016)
Juicebox Provides a Visualization System for Hi-C Contact Maps with Unlimited Zoom
Neva C. Durand et al.
CELL SYSTEMS (2016)
Whole Arm Deletions of 18p: Medical and Developmental Effects
Courtney Sebold et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2015)
A review of 18p deletions
Minire Hasi-Zogaj et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2015)
Genome-wide Maps of Nuclear Lamina Interactions in Single Human Cells
Jop Kind et al.
CELL (2015)
A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
Suhas S. P. Rao et al.
CELL (2014)
Narrowing the localization of the region breakpoint in most frequent Robertsonian translocations
Malgorzata Jarmuz-Szymczak et al.
CHROMOSOME RESEARCH (2014)
A cytogenetic survey of 14,069 newborn infants
J. L. Hamerton et al.
CLINICAL GENETICS (2010)
Centromeric alpha-Satellite DNA Break in Reciprocal Translocations
J. -C. Wang et al.
CYTOGENETIC AND GENOME RESEARCH (2009)
Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship?
Sara Lissoni et al.
MOLECULAR CYTOGENETICS (2009)
Distribution of breakpoints on chromosome 18 in breast, colorectal, and pancreatic carcinoma cell lines
AE Alsop et al.
CANCER GENETICS AND CYTOGENETICS (2006)
The 200-kb segmental duplication on human chromosome 21 originates from a pericentromeric dissemination involving human chromosomes 2, 18 and 13
G Golfier et al.
GENE (2003)
Molecular characterization of 18p deletions: Evidence for a breakpoint cluster
RL Schaub et al.
GENETICS IN MEDICINE (2002)
Non-random radial higher-order chromatin arrangements in nuclei of diploid human cells
M Cremer et al.
CHROMOSOME RESEARCH (2001)
Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p
EM McGhee et al.
CLINICAL GENETICS (2001)