These panels can detect sequence variants,
deletions, and duplications in a significant
number of genes that have been linked to
various conditions leading to infertility in men.
This panel uses Next Generation Sequencing (NGS) technology to analyse coding regions and splicing junctions of genes that may contribute to various infertility issues.
Y chromosome microdeletion (YCM) is a family of genetic disorders caused by missing genes in the
Y chromosome.
Screening for recurrent pregnancy loss
involves testing for underlying genetic,
hormonal, anatomical, or immune factors
that may contribute to repeated miscarriages.
A Genetic Testing before marriage to determine if they are carriers of genes for certain hereditary disorders.
DNA extraction is the process of isolating DNA
from cells, while maternal cell contamination
occurs when maternal DNA contaminates fetal
DNA samples, potentially leading to inaccurate
test results.
Embryo sex selection is a process used to choose the sex of a baby by selecting embryos with the desired gender before implantation during in vitro fertilization (IVF).
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