Related references
Note: Only part of the references are listed.Complex chromosomal rearrangements in infertile males: complexity of rearrangement affects spermatogenesis
Ji Won Kim et al.
FERTILITY AND STERILITY (2011)
Complex and cryptic chromosomal rearrangements involving the MLL gene in acute leukemia: A study of 7 patients and review of the literature
Etienne De Braekeleer et al.
BLOOD CELLS MOLECULES AND DISEASES (2010)
Complex chromosome rearrangements:Report of a new case and literature review
G. S. Pai et al.
CLINICAL GENETICS (2010)
Complex chromosomal rearrangements: some breakpoints may have cellular adaptive significance
Iosif W. Lurie et al.
CLINICAL GENETICS (2010)
Familial balanced (7;11;21)translocation and Down's syndrome in two siblings
E. Schwinger et al.
CLINICAL GENETICS (2010)
Complex five-break rearrangement
Margaret G. Fitzgerald
CLINICAL GENETICS (2010)
A cytogenetic survey of 14,069 newborn infants
J. L. Hamerton et al.
CLINICAL GENETICS (2010)
Combined FISH and PRINS sperm analysis of complex chromosome rearrangement t(1;19;13): an approach facilitating PGD
V. Loup et al.
MOLECULAR HUMAN REPRODUCTION (2010)
Enhanced genomic instabilities caused by deregulated microtubule dynamics and chromosome segregation: a perspective from genetic studies in mice
Chinthalapally V. Rao et al.
CARCINOGENESIS (2009)
Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient
Lucia Ballarati et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2009)
Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: Array CGH study of 47 unrelated cases
Caroline Schluth-Bolard et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2009)
A de novo complex chromosome rearrangement involving three chromosomes (2, 13, and 18) in an oligospermic male
Emel Ergul et al.
FERTILITY AND STERILITY (2009)
Chromosomal instability mediated by non-B DNA: Cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans
Hidehito Inagaki et al.
GENOME RESEARCH (2009)
Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching
Claudia M. B. Carvalho et al.
HUMAN MOLECULAR GENETICS (2009)
Expression profiling of DNA repair genes in human oocytes and blastocysts using microarrays
Souraya Jaroudi et al.
HUMAN REPRODUCTION (2009)
Complex chromosomal rearrangement involving chromosomes 1, 4 and 22 in an infertile male: case report and literature review
I. Salahshourifar et al.
JOURNAL OF APPLIED GENETICS (2009)
Array-CGH detection of three cryptic submicroscopic imbalances in a complex chromosome rearrangement
Yanliang Zhang et al.
JOURNAL OF GENETICS (2009)
Recent advance in our understanding of the molecular nature of chromosomal abnormalities
Hiroki Kurahashi et al.
JOURNAL OF HUMAN GENETICS (2009)
Chromosome instability is common in human cleavage-stage embryos
Evelyne Vanneste et al.
NATURE MEDICINE (2009)
De novo balanced chromosome rearrangements in prenatal diagnosis
Daniela Giardino et al.
PRENATAL DIAGNOSIS (2009)
Complex human chromosomal and genomic rearrangements
Feng Zhang et al.
TRENDS IN GENETICS (2009)
Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report
Roland Haj et al.
MOLECULAR CYTOGENETICS (2009)
Meiotic segregation and interchromosomal effect in the sperm of a double translocation carrier: a case report
Maria S. Juchniuk de Vozzi et al.
MOLECULAR CYTOGENETICS (2009)
Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: case report
Paula J. P. de Vree et al.
MOLECULAR CYTOGENETICS (2009)
A Microhomology-Mediated Break-Induced Replication Model for the Origin of Human Copy Number Variation
P. J. Hastings et al.
PLOS GENETICS (2009)
FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormality
J. A. Fantes et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Breakpoint mapping and array CGH in translocations: Comparison of a phenotypically normal and an abnormal cohort
Julia Baptista et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
A healthy live birth after successful preimplantation genetic diagnosis for carriers of complex chromosome rearrangements
Chun Kyu Lim et al.
FERTILITY AND STERILITY (2008)
Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13)
Marzena Gajecka et al.
GENOME RESEARCH (2008)
Two different forms of palindrome resolution in the human genome: deletion or translocation
Takema Kato et al.
HUMAN MOLECULAR GENETICS (2008)
Gene expression profiling of human oocytes following in vivo or in vitro maturation
Gayle M. Jones et al.
HUMAN REPRODUCTION (2008)
Molecular definition of high-resolution multicolor banding probes: First within the human DNA sequence anchored FISH banding probe set
Anja Weise et al.
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY (2008)
Genome instability: a mechanistic view of its causes and consequences
Andres Aguilera et al.
NATURE REVIEWS GENETICS (2008)
Prenatal diagnosis of monosomy 18p involving a jumping translocation
Sandra Edwards et al.
PRENATAL DIAGNOSIS (2008)
Proteins involved in meiotic recombination: A role in male infertility?
Matthew L. Sanderson et al.
SYSTEMS BIOLOGY IN REPRODUCTIVE MEDICINE (2008)
Further delineation of complex chromosomal rearrangements in fertile male using multicolor banding
Nilufer Karadeniz et al.
MOLECULAR CYTOGENETICS (2008)
Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype
Carolina Sismani et al.
MOLECULAR CYTOGENETICS (2008)
The mechanism of human nonhomologous DNA end joining
Michael R. Lieber
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders
Jennifer A. Lee et al.
CELL (2007)
Nuclear architecture:: Is it important for genome function and can we prove it?
Julio Mateos-Langerak et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2007)
Abnormal meiotic recombination in infertile men and its association with sperm aneuploidy
Kyle A. Ferguson et al.
HUMAN MOLECULAR GENETICS (2007)
Cryptic deletions are a common finding in balanced'' reciprocal and complex chromosome rearrangements: A study of 59 patients
M. De Gregori et al.
JOURNAL OF MEDICAL GENETICS (2007)
Break-induced replication and telomerase-independent telomere maintenance require Pol32
John R. Lydeard et al.
NATURE (2007)
Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies
L. E. L. M. Vissers et al.
HUMAN GENETICS (2007)
Template switching during break-induced replication
Catherine E. Smith et al.
NATURE (2007)
Complex chromosomal rearrangement and intracytoplasmic sperm injection:: A Case Report
G. Joly-Helas et al.
HUMAN REPRODUCTION (2007)
An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype
Iris Bartels et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2007)
A palindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies
Anthony L. Gotter et al.
GENOME RESEARCH (2007)
Constitutional complex chromosomal rearrangements in azoospermic men - Case report and literature review
I-Wen Lee et al.
UROLOGY (2006)
Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriers
Marzena Gajecka et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2006)
Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations
Marzena Gajecka et al.
HUMAN GENETICS (2006)
The transcriptome of human oocytes
Arif Murat Kocabas et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development
Houda Kannous-Benailly et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2006)
Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs
D Giardino et al.
PRENATAL DIAGNOSIS (2006)
Parental and chromosomal origin of unbalanced de novo structural chromosome abnormalities in man
NS Thomas et al.
HUMAN GENETICS (2006)
On the mechanism of gene amplification induced under stress in Escherichia coli
Andrew Slack et al.
PLOS GENETICS (2006)
Micro-array analyses decipher exceptional complex familial chromosomal rearrangement
C Fauth et al.
HUMAN GENETICS (2006)
Analysis of gene expression in single human oocytes and preimplantation embryos
SSL Li et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2),dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements
CP Chen et al.
PRENATAL DIAGNOSIS (2006)
Meiotic recombination and spatial proximity in the etiology of the recurrent t(11;22)
Terry Ashley et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Studying meiosis: a review of. FISH and M-FISH techniques used in the analysis of meiotic processes in humans
M. Oliver-Bonet et al.
CYTOGENETIC AND GENOME RESEARCH (2006)
Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13
T de Ravel et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2005)
Array CGH detection of a cryptic deletion in a complex chromosome rearrangement
C Rosenberg et al.
HUMAN GENETICS (2005)
A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for intracytoplasmatic sperm injection
A Kuechler et al.
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY (2005)
Meiotic spindle checkpoints for assessment of aneuploid oocytes
N Steuerwald
CYTOGENETIC AND GENOME RESEARCH (2005)
Frequency and distribution of chromosome abnormalities in human spermatozoa
C Templado et al.
CYTOGENETIC AND GENOME RESEARCH (2005)
Male infertility in reciprocal translocation carriers: the sex body affair
M Oliver-Bonet et al.
CYTOGENETIC AND GENOME RESEARCH (2005)
Somatic chromosomal abnormalities in infertile men and women
UA Mau-Holzmann
CYTOGENETIC AND GENOME RESEARCH (2005)
Effect of paternal age on the frequency of cytogenetic abnormalities in human spermatozoa
A Buwe et al.
CYTOGENETIC AND GENOME RESEARCH (2005)
The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes
SM Gribble et al.
JOURNAL OF MEDICAL GENETICS (2005)
Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease
CJ Shaw et al.
HUMAN MOLECULAR GENETICS (2004)
Prenatal diagnosis of an extra der(4) resulting from a complex maternal chromosome translocation
MV Migliori et al.
PRENATAL DIAGNOSIS (2004)
Delineation of complex chromosomal rearrangements: evidence for increased complexity
C Astbury et al.
HUMAN GENETICS (2004)
Two unusual chromosome aberrations ascertained by sonographic anomalies
S Bourthoumieu et al.
PRENATAL DIAGNOSIS (2004)
Breakpoints of gross deletions coincide with non-B DNA conformations
A Bacolla et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Fluorescence in situ hybridization characterization of apparently balanced translocation reveals cryptic complex chromosomal rearrangements with unexpected level of complexity
PC Patsalis et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2004)
The human protein translin specifically binds single-stranded microsatellite repeats, d(GT)n, and G-strand telomeric repeats, d(TTAGGG)n:: A study of the binding parameters
E Jacob et al.
JOURNAL OF MOLECULAR BIOLOGY (2004)
The unique transcriptome through day 3 of human preimplantation development
AT Dobson et al.
HUMAN MOLECULAR GENETICS (2004)
A constitutional complex chromosome rearrangement involving meiotic arrest in an azoospermic male: Case report
R Coco et al.
HUMAN REPRODUCTION (2004)
A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2
AL Gotter et al.
HUMAN MOLECULAR GENETICS (2004)
Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements
BC Ballif et al.
HUMAN GENETICS (2004)
A balanced complex chromosomal rearrangement (BCCR) in a family with reproductive failure
J Lespinasse et al.
HUMAN REPRODUCTION (2003)
Spatial proximity of translocation-prone gene loci in human lymphomas
JJ Roix et al.
NATURE GENETICS (2003)
Distance from the chromosome end determines the efficiency of double strand break repair in subtelomeres of haploid yeast
M Ricchetti et al.
JOURNAL OF MOLECULAR BIOLOGY (2003)
Translocation and gross deletion breakpolints in human inherited disease and cancer I: Nucleotide composition and recomblination-assocliated motifs
SS Abeysinghe et al.
HUMAN MUTATION (2003)
Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding method
A Weise et al.
CYTOGENETIC AND GENOME RESEARCH (2003)
A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q24 -> 1q22 and partial monosomy 4q27 -> q28
U Grasshoff et al.
CYTOGENETIC AND GENOME RESEARCH (2003)
Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities
GO Ness et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
A role for the octameric ring protein, Translin, in mitotic cell division
R Ishida et al.
FEBS LETTERS (2002)
The molecular foundations of the maternal to zygotic transition in the preimplantation embryo
RM Schultz
HUMAN REPRODUCTION UPDATE (2002)
Familial complex chromosomal rearrangement resulting in a recombinant chromosome
SA Berend et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
Prenatal diagnosis of a familial complex chromosomal rearrangement involving chromosomes 5, 10, 16 and 18
MH Lee et al.
PRENATAL DIAGNOSIS (2002)
Multicolour spectral karyotyping for complex chromosomal rearrangements in repeated abortion or congenital anomalies
M Tanemura et al.
PRENATAL DIAGNOSIS (2001)
Delayed replication timing leads to delayed mitotic chromosome condensation and chromosomal instability of chromosome translocations
L Smith et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
Unexpected high rate of de novo constitutional t(11;22) translocations in sperm from normal males
H Kurahashi et al.
NATURE GENETICS (2001)
A complex chromosome rearrangement involving chromosome 8, 11, and 12 analyzed by conventional cytogenetic investigations, fluorescence in situ hybridisation, and spectral karyotyping
D Kotzot et al.
ANNALES DE GENETIQUE (2001)
A case with balanced chromosome rearrangement involving chromosomes 9, 14, and 13 in a woman with recurrent abortion
SK Kim et al.
YONSEI MEDICAL JOURNAL (2001)
Chromosome territories, nuclear architecture and gene regulation in mammalian cells
T Cremer et al.
NATURE REVIEWS GENETICS (2001)
Stable non-Robertsonian dicentric chromosomes: four new cases and a review
E Lemyre et al.
JOURNAL OF MEDICAL GENETICS (2001)
HC Forum (R): a web site based on an international human cytogenetic database
O Cohen et al.
NUCLEIC ACIDS RESEARCH (2001)
A de novo complex chromosomal rearrangement with a translocation 7;9 and 8q insertion in a male carrier with no infertility
T Cai et al.
HUMAN REPRODUCTION (2001)
Interchromosomal insertions - Identification of five cases and a review
JO Van Hemel et al.
HUMAN GENETICS (2000)
Frequent chromosomal translocations induced by DNA double-strand breaks
C Richardson et al.
NATURE (2000)
The nonhomologous end-joining pathway of DNA repair is required for genomic stability and the suppression of translocations
DO Ferguson et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)