Question

D: Human Karyotype Analysis: Looking at the set of human karyotypes in lab, match which karyotype (indicated by letters A-L) carries the following descriptions. For "Description", indicate the number of chromosomes, sex of individual, and note about genetic condition (see example below for normal male and female, and see matching Karyotypes for descriptions). Description Letter (A-L) 1. Normal Human Female Karyotype: 46, XX ___ 2. Normal Human Male Karyotype: 46, XY _ Autosomal Non-disjunctions 3. Downs Syndrome (Trisomy 21) ___ _ 4. Edward's Syndrome (Trisomy 18) ___ _ 5. Patau's Syndrome (Trisomy 13) ___ _ Non-disjunction of the Sex Chromosomes 6. Turner's Syndrome (Monosomy X) ___ _ 7. Trisomy X ___ _ 8. Jacob's Syndrome (XYY) ___ _ 9. Klinefelter's Syndrome (XXY) ___ _ Chromosomal rearrangements, insertions, or deletion Letter: 10. Cri-du-Chat (deletion on Chr.5) 46, XY del[5] _ 11. Fragile X (Expansion of X Chromosome) 46, X,fra(X) _ 12. Philadelphia Chromosome, _ _ (Translocation between Chromosomes 9 and 22)

          D: Human Karyotype Analysis:

Looking at the set of human karyotypes in lab, match which karyotype (indicated by letters A-L) carries the following descriptions. For "Description", indicate the number of chromosomes, sex of individual, and note about genetic condition (see example below for normal male and female, and see matching Karyotypes for descriptions).

Description Letter (A-L)
1. Normal Human Female Karyotype: 46, XX _______
2. Normal Human Male Karyotype: 46, XY _______

Autosomal Non-disjunctions
3. Downs Syndrome (Trisomy 21) _________ _______
4. Edward's Syndrome (Trisomy 18) _________ _______
5. Patau's Syndrome (Trisomy 13) _________ _______

Non-disjunction of the Sex Chromosomes
6. Turner's Syndrome (Monosomy X) _________ _______
7. Trisomy X _________ _______
8. Jacob's Syndrome (XYY) _________ _______
9. Klinefelter's Syndrome (XXY) _________ _______

Chromosomal rearrangements, insertions, or deletion Letter:
10. Cri-du-Chat (deletion on Chr.5) 46, XY del[5] _______
11. Fragile X (Expansion of X Chromosome) 46, X,fra(X) _______
12. Philadelphia Chromosome, _________ _______
(Translocation between Chromosomes 9 and 22)

D: Human Karyotype Analysis:

Looking at the set of human karyotypes in lab, match which karyotype (indicated by letters A-L) carries the following descriptions. For "Description", indicate the number of chromosomes, sex of individual, and note about genetic condition (see example below for normal male and female, and see matching Karyotypes for descriptions).

Description Letter (A-L)
1. Normal Human Female Karyotype: 46, XX
2. Normal Human Male Karyotype: 46, XY

Autosomal Non-disjunctions
3. Downs Syndrome (Trisomy 21)
4. Edward's Syndrome (Trisomy 18)
5. Patau's Syndrome (Trisomy 13)

Non-disjunction of the Sex Chromosomes
6. Turner's Syndrome (Monosomy X)
7. Trisomy X
8. Jacob's Syndrome (XYY)
9. Klinefelter's Syndrome (XXY)

Chromosomal rearrangements, insertions, or deletion Letter:
10. Cri-du-Chat (deletion on Chr.5) 46, XY del[5]
11. Fragile X (Expansion of X Chromosome) 46, X,fra(X)
12. Philadelphia Chromosome,
(Translocation between Chromosomes 9 and 22)

Added by Melissa R.

Question

Please give Ace some feedback