Madysen Buckley
Mrs.Hays
Biology Honors
I. For my Baby Lab that we had done in class, my daughter, Taylor Mehl, had
Rachel and I such as her freckles, nose size, hair curliness, and eyelash length.
Taylors, freckles, which both Rachel and I have, turned out to be homozygous
dominant, as well as her nose size, hair curliness and eyelash length. Taylors
freckles were present and her nose was a small, round button. Also, her hair,
just as her parents, was straight and her eyelashes were short, just like
Rachels.
III. One trait that Taylor had inherited, incomplete dominance wise, from Rachel
and I was her eye color. Incomplete dominance is when some heterozygous
genotype had been mixed with B-Brown eyes, and b-blue eyes, which created
her very own genotype, Bb. This combination led to the phenotype oh her
Polygenic trait is a trait that is coded for by more than one allele. Taylors
A A
VI. In my karyotype, the disease that is indicated is Down Syndrome. The way I
AA AA can tell Taylor has Down Syndrome is that she has one more
of Down Syndrome are flattened facial features, a small head, short neck,
protruding tongue, ect. The prognosis, or long-term outcome, for Taylor will
possibly not living past age fifty as well as a long-term learning and social
disability. The type of assistance and treatment Taylor will need in her future
development help, help with her speech, help with learning numbers, and