Genomic imprinting is an epigenetic phenomenon of monoallelic gene expression pattern
depending on parental origin. In humans, congenital imprinting disruptions resulting from …

Chromosomal polymorphism plays a major role in speciation processes in mammals with
high rates of karyotypic evolution, as observed in the family Cervidae. One remarkable …

Background and Objectives: Recurrent pregnancy loss (RPL) affects numerous couples
worldwide and has traditionally been attributed mainly to maternal factors. However, recent …

Background Robertsonian translocations are common structural rearrangements and confer
an increased genetic reproductive risk due to the formation of trivalent structure during …

Background Carriers of reciprocal translocations often have more unbalanced spermatozoa
and higher DNA fragmentation rates, elevating reproductive risk. The simple swim‐up …

Fluorescence in situ hybridization analysis of numerical chromosomal abnormalities in the
sperm of Robertsonian translocation der (13; 14)(q10; q10) carriers has focused on a limited …

The genus Mazama stands out among the Neotropical deer due to their wide intra and
interspecific karyotypic diversification, which is associated with an accentuated …

Background: Robertsonian translocations (RobTs) are one of the major chromosomal
abnormalities which lead to spontaneous abortion. They occur in the human population at …

As women age, reproductive challenges become more prevalent, including increased
miscarriage rates due to genetic defects, as well as common complications of the pregnancy …

Robertsonian translocations (RTs) are very common balanced structural chromosome
rearrangements in humans. Due to alterations in the chromosome segregation pattern and …