Gregor Mendel
Phenotype
Genotype
Chromatids
Centromere
Diploid
Chromosomes characterized by
Karyotype
how many of the 23 pairs of chromosomes are autosomes (homologous)?
Remaining pair of sex chromosomes
1/23
Genotype
Meiosis
haploid
Mitosis
Meiosis
Allele
Codominant
Monogenic traits
Polygenic traits
Mutation
if double stranded breaks
Types of DNA mutation
Point mutation
Frameshift mutation
Mendelian Single-Gene Disorders results from
Pedigree
Translocation
Autosomal recessive example
Sex-linked
who is more impacted by sex-linked medelian disorder?
Aneuploidy
Inversion
Deletion
Trisomy 21 is known as
down syndrome
Klinefelter Syndrome
Turner Syndrome
Monosomy X
Rarely survive birth