Unit 3 Chapter 3 (1st Secondary) Biology
Maternal grandfather
Maternal grandmother
Paternal grandfather
Paternal grandmother
Sex-linked recessive
Sex-linked dominant
Autosomal recessive
Autosomal dominant
Gene therapy for normalizing blood glucose levels
Genetic testing for hemophilia
Genetic testing for typhoid disease
Evolutionary relationship
In the karyotype of somatic cells
In the DNA finger print
In the structure of the chromosome
In the function of the protein formed by that gene
Colour blind male
Hemophiliac male.
Tall Pea plant
Female carrier for colour-blindness.
Haemophilic and colour blind daughters
All sons and daughters are haemophilic and colour blind
50% haemophilic, colour blind sons and 50% normal sons
50% haemophilic, colour blind sons and 50% normal daughters
Triple-X syndrome
A woman with only one sex chromosome
A woman with Down's syndrome
XYY syndrome
All your cells have the same genome, but different parts are active in different cells.
Your cells have different genome, and different parts are active in different cells.
All your cells have the same genome and all parts of the genome are active in all cells.
Your cells have different genome and all parts of the genome are active in all cells.
XY
XO
XX
XXX
50% daughter will be normal and 50% son will be hemophiliac.
All daughters will be carriers and all sons will be normal.
All daughters will be normal and all sons will be carrier.
50% daughter will be hemophiliac and 50% son will be normal.
Upward slanting eyes.
Small head and ears
Taller than average height
An extra copy of chromosome 21
1 is X'Y and 2 is XX'
1 is X'Y and 2 is X'X'
1 is XY and 2 is XX'
1 is XY and 2 is X'X'
(22 + X) and (22 + X)
(22 + XX) and (22 + 0)
(22 + X) and (23 + X)
(22 + X) and (22 + XX)
XY
XO
XXX
XX
46
22
23
44
Female with Down's syndrome
Female with Turner's syndrome
Male with a Down's syndrome
Male with Klinefelter's syndrome
Colour of feathers in Andalusian Fowls
Fur colour in mice
Blood groups in Man
Eyes colour in Drosophila
Sex-limited trait
Sex-linked trait
Sex-influenced trait
Mendelian trait
Shape
Size
Number of genes it carries
All the previous
Klinefelter's syndrome
Turner's syndrome
Down's syndrome
Normal male
22 + X
22 + Y
44 + O
44 + Y
50
25
Zero
100
Colour blindness
Haemophilia
Early (genetic) baldness
Infantile paralysis
Early baldness
Appearance of beard
Colour blindness
Haemophilia
22 + XY
22 + Y
23 + Y
23 + X
White eyed male
White eyed female
Red eyed male
Red eyed female
B+ B
B B
B B+
B+ B+
Sex linked dominant
Sex linked recessive
Autosomal dominant
Autosomal recessive
Male, 1st
Male, 2nd
Female, 1st
Female, 2nd
B+BXRXR x B+BXRY
B+BXRXr x BBXRY
B+BXrXr x BBXRrY
B+B+XRXR x BBXRY
ZGZG and ZgW
ZGZg and ZgW
ZgZg and ZGW
ZGZg and ZGW
46
23
1
2
44 + XX
22 + XY
22 + X
All the previous
Colour blindness
Appearance of beard
Genetic baldness
Eye colour in human beings
All of the males
All of the females
Half of the females
Half of the males
A hemophiliac mother and an unaffected father
A carrier mother and an unaffected father
A carrier mother and a hemophiliac father
An unaffected, non-carrier mother and a hemophiliac father
X chromosome
Y chromosome
X and Y chromosomes
Autosomes
25%
Zero %
50%
100%
Sex-linked genes
Sex-influenced genes
Sexual disorders
Sex-limited genes
Father is colour blind and mother is carrier for the disease
Both father and mother are normal
Mother is carrier for the disease and father is normal
Father is colour blind and mother is normal
25%
50%
75%
Zero %
They 44 chromosomes
They carry genes for sex-linked characters
They carry genes for sex influenced characters
They are of different size
A and C
D and C
A and B
B and D
Companion cell in phloem tissue
Parenchyma cell
The egg of Ostrich
A cell in the ovarian wall in Drosophila
Down’s syndrome
Klinefilter syndrome
Triple-X syndrome
Turner syndrome
Salinity of water
Presence of X chromosome
Environmental conditions
The Y chromosome
Three
Four
Five
Six
Recessive trait
Dominant trait
Sex-linked trait
Sex-limited trait
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