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kmstewart 2016
Homozygous or heterozygous
dominant?
Chi-squared values
2013 P2 #2
2003 P1 #7
F1 Parents
Brown x Brown
F2 Progeny
84 Brown
Yellow x Yellow
23 Brown
61 Yellow
CoDominance!
2001 P1 #9
Name
Mr.
Bibbon
Mrs.
Bibbon
Mr.
Ribbon
Mrs.
Ribbon
Baby
Mary
Baby John
Phenotype
(Blood type)
O
AB
B
B
A
O
Karyotype
2004 P1 #7
(a) Define the following terms: (i) Sex linkage [2] (ii) Allele [2]
(b) In humans, a recessive X-linked mutation, g, causes green
defective colour-vision. Robert and Sheila, both with normal
colour vision, G, have three children John, Mary and Betty.
Betty and Mary have normal colour vision, but John has
abnormal colour vision. John, Mary and Betty marry spouses with
normal vision. John has a daughter with normal vision. Mary has
one son with abnormal vision and two sons with normal vision.
Betty has six sons with normal vision.
In Table 5, give the most likely genotype for the persons in this
family, by inserting the G/g alleles present in EACH individual.
[6]
Name
Genotype
Parents
Robert
Sheila
John
Mary
Betty
Johns daughter
Children
Grandchildr
en
Colour-blindness inheritance
Dihybrid
Inheritanc
e
Dihybrid Inheritance