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38 Cards in this Set

  • Front
  • Back

traits that don't follow the rules

Non-Mendelian Traits

multiple genes coding for a trait

Polygenes

the third phenotype is a blending of the 1st and 2nd phenotype

Incomplete Dominance

the third phenotype is a presence of both the 1st and 2nd phenotype

Codominance

multiple concepts of heredity

Multiple Alleles

sex linked trait present in the Y chromosome

Holandric Trait

traits that are present in the sex chromosomes

Sex Linked Traits

blood disorder where the blood does not clot properly

Hemophilia

organisms that undergo selective breeding

transgenic organisms

part of a bacteria

plasmid

breeding only those with desirable traits

selective breeding

plasmid + foreign DNA

Recombinant DNA

EDWARD 3 MAJOR SYMPTOMS

FLEXED BIG TOE


MALFORMED EARS


SMALL MOUTH

EDWARD PREVALENCE

ONE IN 6,000

EDWARD LIFE EXPECTANCY

50% DIE BEYOND FIRST TO SIX DAYS


MAJORITY DIE BEFORE BIRTH

EDWARD CHROMOSOMAL ABNORMALITY

TRISOMY 18



DOWN SYNDROME SYMPTOMS

REDUCED MUSCLE TONE


FLAT NASAL BRIDGE


BELOW AVERAGE WEIGHT AND LENGTH AT BIRTH

DOWN SYNDROME PREVALENCE

1 IN EVERY 700

DOWN SYNDROME LIFE EXPECTANCY

ABOUT 10 YRS OLD

DOWN SYNDROME ABNORMALITY

TRISOMY 21

MPB SYMPTOMS

HAIRLINE FORMS M SHAPE


HAIRLINE MOVES BACKWARD


HAIR BECOMES FINER, SHORTER, THINNER

MPB PREVALENCE

50% of men over age of 50

ANGELMAN PREVALENCE

1 IN 20,000

ANGELMAN SYMPTOMS

DELAYED DEVELOPMENT


FREQUENT SMILING AND LAUGHTER


INTELLECTUAL DISABILITY



ANGELMAN CHROMOSOMAL AB

ABSENCE OF GENES ON CHROMOSOME 15

KLINEFELTER SYMPTOMS

LARGER BREAST


LOWER ENERGY LEVEL


SMALLER TESTICLES/PENIS

KLINEFELTER PREVALENCE

1 IN 500-1,000

KLINEFELTER CHROMOSOMAL ABNORMALITY

TRISOMY X

CAT CRY SYMPTOMS

ABNORMALLY SHAPED EARS


SMALL HEAD


SOUNDS LIKE A CAT

CAT CRY PREVALENCE

1 IN 50,000

CAT'S CRY CHROMOSOMAL ABNORMALITY

missing piece of chromosome 5

CF SYMPTOMS

WHEEZING


REPEATED LUNG INFECTIONS


MALE INFERTILITY

CF PREVALENCE

APPROX 1,000 CASES OF CF EACH YEAR

CF CHROMOSOMAL ABNORMALITY

CAUSED BY MUTATIONS IN CFTR GENE

CF AVE LIFE SPAN

ABOUT 37 YRS

TURNERS SYMPTOMS

SHIELD CHEST


WEBBED NECK


RUDIMENTARY OVARIES



TURNERS CHROMOSOMAL ABNORMALITY

MONOSOMY X

TURNERS PREVALENCE

50 PER 100,000