Most rare diseases are caused by genetics. A molecular genetic diagnosis can be made more quickly and readily by identifying the underlying genetic change, for instance by exome sequencing (ES). The analysis of every region of our DNA that codes for a protein is known as ES.
Understanding the many different genetic causes of childhood-onset hearing loss suggests that genomic testing could aid in treatment planning, including optimal treatment timing.
Understanding the many different genetic causes of childhood-onset hearing loss suggests that genomic testing could aid in treatment planning, including optimal treatment timing.
Advances in understanding the diverse genetic causes of childhood-onset hearing loss suggest that genomic testing could help with treatment planning, including appropriate therapy timing.
Advances in understanding the many different genetic causes of childhood-onset hearing loss indicate that genomic testing could assist in treatment planning, including optimal timing of treatment.
New Delhi [India], November 22 (ANI/GPRC): "Save the Sibling" is a concept oriented unique bouquet of services with substantial financial reimbursement, which would be available as a package, for the first time ever in the country, if not the world.
Bengaluru (Karnataka) [India], March 30 (ANI/PNN): In a first-of-its-kind multidimensional IVF treatment in the country, Khushi Fertility and IVF Centre, a pioneering Bengaluru -based fertility centre specialising in the latest Assisted Reproductive Technologies (ART) implemented Clinical Ex