Balanced chromosomal rearrangements represent one of the most common forms of genetic abnormality affecting approximately 1 in every 500 (0.2%) individuals. Difficulties processing the abnormal chromosomes during meiosis lead to an elevated risk of chromosomally abnormal gametes, resulting in high rates of miscarriage and/or children with congenital abnormalities. It has also been suggested that the presence of chromosome rearrangements may also cause an increase in aneuploidy affecting structurally normal chromosomes, due to disruption of chromosome alignment on the spindle or disturbance of other factors related to meiotic chromosome segregation. The existence of such a phenomenon (an inter-chromosomal effect—ICE) remains controversial, w...
Despite the clinical importance of aneuploidy, surprisingly little is known concerning its impact du...
<div><p>Whole-chromosome imbalances affect over half of early human embryos and are the leading caus...
Abstract Background Infertility is a natural mechanis...
In translocation carriers, the presence of aneuploidy for the chromosomes unrelated to the rearrange...
<div><p>The objective of this study was to investigate the frequency and type of chromosome segregat...
The objective of this study was to investigate the frequency and type of chromosome segregation patt...
The frequency of the Robertonian (ROB) translocation in newborn babies is approximately one in 1000....
Male carriers of chromosomal abnormalities (CA) are more frequent in the infertile population. These...
Translocation is a type of chromosomal abnormality, which results in a chromosome breaks where the p...
The first cell cycles following in vitro fertilization (IVF) of human gametes are prone to chromosom...
Robertsonian translocations (RTs) are amongst the most common chromosome abnormalities, but being es...
Abstract Chromoanagenesis is a cellular mechanism that leads to complex chromosomal rearrangements (...
It has been estimated that as much as 70-80% of all human conceptions do not develop to term. A majo...
Purpose To demonstrate that translocation carrier patients can be identified by analysis of chromoso...
Preimplantation genetic diagnosis (PGD) involves the genetic screening of cleavage-stage embryos gen...
Despite the clinical importance of aneuploidy, surprisingly little is known concerning its impact du...
<div><p>Whole-chromosome imbalances affect over half of early human embryos and are the leading caus...
Abstract Background Infertility is a natural mechanis...
In translocation carriers, the presence of aneuploidy for the chromosomes unrelated to the rearrange...
<div><p>The objective of this study was to investigate the frequency and type of chromosome segregat...
The objective of this study was to investigate the frequency and type of chromosome segregation patt...
The frequency of the Robertonian (ROB) translocation in newborn babies is approximately one in 1000....
Male carriers of chromosomal abnormalities (CA) are more frequent in the infertile population. These...
Translocation is a type of chromosomal abnormality, which results in a chromosome breaks where the p...
The first cell cycles following in vitro fertilization (IVF) of human gametes are prone to chromosom...
Robertsonian translocations (RTs) are amongst the most common chromosome abnormalities, but being es...
Abstract Chromoanagenesis is a cellular mechanism that leads to complex chromosomal rearrangements (...
It has been estimated that as much as 70-80% of all human conceptions do not develop to term. A majo...
Purpose To demonstrate that translocation carrier patients can be identified by analysis of chromoso...
Preimplantation genetic diagnosis (PGD) involves the genetic screening of cleavage-stage embryos gen...
Despite the clinical importance of aneuploidy, surprisingly little is known concerning its impact du...
<div><p>Whole-chromosome imbalances affect over half of early human embryos and are the leading caus...
Abstract Background Infertility is a natural mechanis...