Results 21 to 30 of about 226,802 (259)
Identification of chromosomes involved in a Robertsonian translocation in cattle [PDF]
Les chromosomes impliqués dans une translocation robertsonienne décrite, tout d’abord, en coloration conventionnelle par Darre et al. (1974) ont été déterminés à l’aide des techniques de marquage G(GTG), R(RBA) et C(CBG). Les chromosomes concernés sont le 9 et le 23.
Durand V +5 more
doaj +6 more sources
Preimplantation genetic diagnosis (PGD) is well established method for treatment of genetic problems associated with infertility. Moreover, PGD with next-generation sequencing (NGS) provide new possibilities for diagnosis and new parameters for ...
Krzysztof Lukaszuk +7 more
doaj +2 more sources
Chromosomal Analysis in <i>Crotophaga ani</i> (Aves, Cuculiformes) Reveals Extensive Genomic Reorganization and an Unusual Z-Autosome Robertsonian Translocation. [PDF]
Although cytogenetics studies in cuckoos (Aves, Cuculiformes) have demonstrated an interesting karyotype variation, such as variations in the chromosome morphology and diploid number, their chromosome organization and evolution, and relation with other ...
Kretschmer R +8 more
europepmc +2 more sources
How much, if anything, do we know about sperm chromosomes of Robertsonian translocation carriers? [PDF]
In men with oligozoospermia, Robertsonian translocations (RobTs) are the most common type of autosomal aberrations. The most commonly occurring types are rob(13;14) and rob(14;21), and other types of RobTs are described as ‘rare’ cases.
Wiland E +3 more
europepmc +2 more sources
Robertsonian translocation in a Chianine cow and in its offspring [PDF]
Maurizio Silvestrelli +3 more
openalex +5 more sources
Reproductive Risk of the Silent Carrier of Robertsonian Translocation
The aim of this study was the evaluation of risk among the couples various types of Robertsonian translocations.Cytogenetic diagnosis has been carried out according to the Moorhead and Seabright method.Cytogenetics diagnosis was performed in 17 couples having Robertsonian translocations.
Jehona Kolgeci +5 more
openaire +4 more sources
Chromosomal Abnormalities in Couples Experiencing Recurrent Implantation Failure in West of Iran: A Case-Control Study. [PDF]
Chromosomal abnormalities significantly contribute to RIF. Therefore, it is imperative to conduct cytogenetic screening for both partners before initiating any assisted reproductive technology procedures. ABSTRACT Background Recurrent Implantation Failure (RIF) is defined as the inability to establish pregnancy despite high‐quality embryo transfer ...
Asgari A +4 more
europepmc +2 more sources
Human-induced pluripotent stem cells (hiPSCs) clones NSi001-A, NSi001-B, and NSi001-C were generated from a female individual of Indian origin having Robertsonian translocation down syndrome (DS) by reprogramming peripheral blood mononuclear cells (PBMCs)
Sunita Nehra +4 more
doaj +1 more source
Prevalence and Phenotypic Impact of Robertsonian Translocations [PDF]
Robertsonian translocations (RTs) result from fusion of 2 acrocentric chromosomes (e.g., 13, 14, 15, 21, 22) and consequential losses of segments of the p arms containing 47S rDNA clusters and transcription factor binding sites. Depending on the position of the breakpoints, the size of these losses vary considerably between types of RTs. The prevalence
Hochstenbach, PFR, Poot, Martin
openaire +4 more sources
Reciprocal translocation and Robertsonian translocation are known to be causative factors of male infertility. However, the association between autosomal reciprocal translocation, Robertsonian translocation and semen parameters remains controversial.
Xiaochuan Chen, Canquan Zhou
semanticscholar +1 more source

