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The genetics laboratory confirmed the trisomic condition in the fetus.

Researchers are studying the trisomic probability of chromosome 18 to identify genetic markers.

Children with trisomic conditions may exhibit physical and cognitive developmental delays.

The doctor suggested genetic testing to rule out trisomic disorders in the newborn.

Trisomic cells often exhibit abnormal cell division during mitosis.

The genetic counselor used trisomic examples to explain potential outcomes in future pregnancies.

The biotech company has developed a new technique to detect trisomic conditions during prenatal screening.

Scientists have identified multiple genes contributing to the trisomic condition in Down syndrome.

The genetic mutation responsible for trisomy 21 is believed to alter the expression of several critical genes.

Trisomic individuals might require special educational programs to support their learning needs.

Geneticists use advanced techniques to diagnose and analyze trisomic disorders in affected individuals.

The incidence of trisomic conditions increases with maternal age, particularly for chromosome 21.

Down syndrome, a well-known trisomic condition, involves three copies of chromosome 21.

Medical advances have improved the outcomes for individuals diagnosed with trisomic disorders.

The study of trisomic embryos can help in understanding the effects of genetic abnormalities on development.

Trisomic conditions often present with unique physical characteristics that aid in diagnosis.

The prenatal screening for trisomic conditions is becoming more accessible and accurate.

The trisomic variation in human genetics is an area of ongoing research with significant implications.

Early intervention strategies for trisomic children are crucial for optimal developmental outcomes.