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What are the three periods of the zygote
WHAT
WHAT
WHAT
What are the three periods of the zygote
Fertilization
Implantation
Germ disk
Fertilization occurs in the WHAT
Fertilization occurs in the FALLOPIAN TUBE
Fertilization
24-30 hours = WHAT
36 hours = WHAT
48 hours = WHAT
3 days = WHAT
4 days = WHAT
Fertilization
24-30 hours = Chromosomes combine
36 hours = zygote divides into 2 cells
48 hours = 4 cells
3 days = 16-32 cells
4 days = Blastocyst of 100 cells
Genetic development
Karyotype = WHAT chromosomes
Sperm and ovum = WHAT chromosomes
Genetic development
Karyotype = 46 chromosomes
Sperm and ovum = 23 chromosomes
Genetic development
Not WHAT of grandparents
WHAT combinations
Genetic development
Not REPLICAS of grandparents
INFINITE combinations
Traits
Traits/Alleles coded WHAT
Traits
Traits/Alleles coded twice
Traits
Genetic code = WHAT
Homozygous = WHAT
Heterozygous = WHAT
Manifestation of trait = WHAT
Traits
Genetic code = Genotype
Homozygous = Matching
Heterozygous = Different
Manifestation of trait = Phenotype
Sex-linked traits
Y-chromosomes = WHAT passed to all WHAT
X-chromosome = WHAT inheritance
Sex-linked traits
Y-chromosomes = All FATHERS passed to all SONS
X-chromosome = COMPLEX inheritance
what does intersex mean
Neither female nor male NOT hermaphrodite
Intersex - 13+ etiologies (causes or forms)
WHAT
WHAT
WHAT
Intersex - 13+ etiologies (causes or forms)
Non-binary (1 in 75)
Ambiguous genitalia (1 in 2000)
Physical, not psychological (1 in 15000)
What are two genetic intersex syndromes
WHAT
WHAT
What are two genetic intersex syndromes
Turner’s syndrome
Klinefelter’s syndrome
Turner’s syndrome
WHAT chromosomes
1 in WHAT “female”
Turner’s syndrome
Xo chromosomes
1 in 2500 “female”
Turner’s syndrome - Phenotypic expression
WHAT
WHAT
WHAT
Turner’s syndrome - Phenotypic expression
Short
Wider neck
Broad chest
Turner’s syndrome - secondary sex characteristics
WHAT
WHAT
WHAT
Turner’s syndrome - secondary sex characteristics
Menstruation
Ovulation
Breast development
Klinefelter’s syndrome
WHAT chromosomes
1 in WHAT “male” births
Klinefelter’s syndrome
XXY chromosomes
1 in 1000 “male” births
Klinefelter’s syndrome - Assigned male at birth
Low WHAT count
WHAT
WHAT development
body WHAT
WHAT distribution
Klinefelter’s syndrome - Assigned male at birth
Low SPERM count
INFERTILITY
BREAST development
body HAIR
FAT distribution
What are the two types of testosterone absorption
WHAT
WHAT
What are the two types of testosterone absorption
Congenital Adrenal Hyperplasia (XX)
Androgen Insensitivity Syndrome (XY)
Congenital Adrenal Hyperplasia (XX)
Affects 1 in WHAT
Congenital Adrenal Hyperplasia (XX)
Affects 1 in 10000
Androgen Insensitivity Syndrome (XY)
Affects 1 in WHAT
Androgen Insensitivity Syndrome (XY)
Affects 1 in 20000
Atypical development
Number of WHAT
Inherited WHAT
Mutated WHAT
Atypical development
Number of CHROMOSOMES
Inherited ALLELES
Mutated ALLELES