184685
Balbiani rings are the structural features of:
1 allosomes
2 autosomes
3 lampbrush chromosomes
4 polytene chromosomes
Explanation:
: Balbiani rings are the structural feature of polytene chromosomes. - Polytene chromosomes were cliscovered by Balbiani in 1882 in larval salivary of Chironimus. - It is specialized interphase chromosomes present in certain insect cells. - Cells with polytene chromosomes undergo repeated rounds of DNA teplication without cell division. - Polytene chromosomes have alternating dark bands and light interbands. bands that are sites of gene expression expand to give chromosome paff (Balbiani rings).
Karnataka CET-2002
Principle of Inheritance and Variation
184687
Gynecomastia is a symptom of
1 Tumer's syndrome
2 Down's syndrome
3 Cri-du-chat syndrome
4 Klinefelter's syudrome
Explanation:
: Gynecomastia is a symptom of Klinefelters syndrome. The presence of 2 X chromosomes causes appearance of femine characters in male. It is triggered by a decreases in the amoum of the hormone testosterone compared with estrogen. - Gynecomastia is a condition where there will be an enlargement of the male breast. - Klinefelter's syntrome is chatacterized by trisomy (XXY). There are 47 chromosomes instead of nomal 46.
Kerala PMT-2008
Principle of Inheritance and Variation
184688
The affected male in the pedigree chart is symbolized by
1234
Show/Hide Explanation
Explanation:
: Shaded square represent the affected male in the pedigree chart. - A pedigree is a family tree or chart made of symbols and lines that represent a person's genetic family history. - In pedigree, symbol represent people and line tepresent genetic relationships.
Karnataka CET-2022
Principle of Inheritance and Variation
184690
Both sickle cell anaemia and Huntingtons chorea are
1 bacteria related diseases
2 congenital disorders
3 pollutant induced disorders
4 virus related diseases
Explanation:
: Both sickle cell anaemia and Huntington's chores are congerital disorder. Congerital disorders can defined as structural or functional abrormalities that occur during intrauterine life. It is also called birth defects. Fickle cell anaemia is autosome linked reccesive trait that can be transmitted from parents to offspring when both the parents are carrier for the gene. Huntington's chored an inherited condition in which nerve cells in the brain break down overtime.
BCECE-2014
Principle of Inheritance and Variation
184691
Absorption of tosic amounts of iron due to a genetically defective control mechanisms is known as
1 Haenatochromatosis
2 Haemosiderosis
3 Haemoptysis
4 Haematoma.
Explanation:
: Absorption of toxic amount of iron due to a gentically defective control mechamism is known as haematochromatosis. It is most common autosomal tecessive genetic disorder and the most common cause of severe iron overload. Hereditary, Haematochromatosis is a disorder that causes the body to absorb too much iron from the diet. The excess iron accumulate in and eventually damages the body tissue and organs.
184685
Balbiani rings are the structural features of:
1 allosomes
2 autosomes
3 lampbrush chromosomes
4 polytene chromosomes
Explanation:
: Balbiani rings are the structural feature of polytene chromosomes. - Polytene chromosomes were cliscovered by Balbiani in 1882 in larval salivary of Chironimus. - It is specialized interphase chromosomes present in certain insect cells. - Cells with polytene chromosomes undergo repeated rounds of DNA teplication without cell division. - Polytene chromosomes have alternating dark bands and light interbands. bands that are sites of gene expression expand to give chromosome paff (Balbiani rings).
Karnataka CET-2002
Principle of Inheritance and Variation
184687
Gynecomastia is a symptom of
1 Tumer's syndrome
2 Down's syndrome
3 Cri-du-chat syndrome
4 Klinefelter's syudrome
Explanation:
: Gynecomastia is a symptom of Klinefelters syndrome. The presence of 2 X chromosomes causes appearance of femine characters in male. It is triggered by a decreases in the amoum of the hormone testosterone compared with estrogen. - Gynecomastia is a condition where there will be an enlargement of the male breast. - Klinefelter's syntrome is chatacterized by trisomy (XXY). There are 47 chromosomes instead of nomal 46.
Kerala PMT-2008
Principle of Inheritance and Variation
184688
The affected male in the pedigree chart is symbolized by
1234
Show/Hide Explanation
Explanation:
: Shaded square represent the affected male in the pedigree chart. - A pedigree is a family tree or chart made of symbols and lines that represent a person's genetic family history. - In pedigree, symbol represent people and line tepresent genetic relationships.
Karnataka CET-2022
Principle of Inheritance and Variation
184690
Both sickle cell anaemia and Huntingtons chorea are
1 bacteria related diseases
2 congenital disorders
3 pollutant induced disorders
4 virus related diseases
Explanation:
: Both sickle cell anaemia and Huntington's chores are congerital disorder. Congerital disorders can defined as structural or functional abrormalities that occur during intrauterine life. It is also called birth defects. Fickle cell anaemia is autosome linked reccesive trait that can be transmitted from parents to offspring when both the parents are carrier for the gene. Huntington's chored an inherited condition in which nerve cells in the brain break down overtime.
BCECE-2014
Principle of Inheritance and Variation
184691
Absorption of tosic amounts of iron due to a genetically defective control mechanisms is known as
1 Haenatochromatosis
2 Haemosiderosis
3 Haemoptysis
4 Haematoma.
Explanation:
: Absorption of toxic amount of iron due to a gentically defective control mechamism is known as haematochromatosis. It is most common autosomal tecessive genetic disorder and the most common cause of severe iron overload. Hereditary, Haematochromatosis is a disorder that causes the body to absorb too much iron from the diet. The excess iron accumulate in and eventually damages the body tissue and organs.
184685
Balbiani rings are the structural features of:
1 allosomes
2 autosomes
3 lampbrush chromosomes
4 polytene chromosomes
Explanation:
: Balbiani rings are the structural feature of polytene chromosomes. - Polytene chromosomes were cliscovered by Balbiani in 1882 in larval salivary of Chironimus. - It is specialized interphase chromosomes present in certain insect cells. - Cells with polytene chromosomes undergo repeated rounds of DNA teplication without cell division. - Polytene chromosomes have alternating dark bands and light interbands. bands that are sites of gene expression expand to give chromosome paff (Balbiani rings).
Karnataka CET-2002
Principle of Inheritance and Variation
184687
Gynecomastia is a symptom of
1 Tumer's syndrome
2 Down's syndrome
3 Cri-du-chat syndrome
4 Klinefelter's syudrome
Explanation:
: Gynecomastia is a symptom of Klinefelters syndrome. The presence of 2 X chromosomes causes appearance of femine characters in male. It is triggered by a decreases in the amoum of the hormone testosterone compared with estrogen. - Gynecomastia is a condition where there will be an enlargement of the male breast. - Klinefelter's syntrome is chatacterized by trisomy (XXY). There are 47 chromosomes instead of nomal 46.
Kerala PMT-2008
Principle of Inheritance and Variation
184688
The affected male in the pedigree chart is symbolized by
1234
Show/Hide Explanation
Explanation:
: Shaded square represent the affected male in the pedigree chart. - A pedigree is a family tree or chart made of symbols and lines that represent a person's genetic family history. - In pedigree, symbol represent people and line tepresent genetic relationships.
Karnataka CET-2022
Principle of Inheritance and Variation
184690
Both sickle cell anaemia and Huntingtons chorea are
1 bacteria related diseases
2 congenital disorders
3 pollutant induced disorders
4 virus related diseases
Explanation:
: Both sickle cell anaemia and Huntington's chores are congerital disorder. Congerital disorders can defined as structural or functional abrormalities that occur during intrauterine life. It is also called birth defects. Fickle cell anaemia is autosome linked reccesive trait that can be transmitted from parents to offspring when both the parents are carrier for the gene. Huntington's chored an inherited condition in which nerve cells in the brain break down overtime.
BCECE-2014
Principle of Inheritance and Variation
184691
Absorption of tosic amounts of iron due to a genetically defective control mechanisms is known as
1 Haenatochromatosis
2 Haemosiderosis
3 Haemoptysis
4 Haematoma.
Explanation:
: Absorption of toxic amount of iron due to a gentically defective control mechamism is known as haematochromatosis. It is most common autosomal tecessive genetic disorder and the most common cause of severe iron overload. Hereditary, Haematochromatosis is a disorder that causes the body to absorb too much iron from the diet. The excess iron accumulate in and eventually damages the body tissue and organs.
184685
Balbiani rings are the structural features of:
1 allosomes
2 autosomes
3 lampbrush chromosomes
4 polytene chromosomes
Explanation:
: Balbiani rings are the structural feature of polytene chromosomes. - Polytene chromosomes were cliscovered by Balbiani in 1882 in larval salivary of Chironimus. - It is specialized interphase chromosomes present in certain insect cells. - Cells with polytene chromosomes undergo repeated rounds of DNA teplication without cell division. - Polytene chromosomes have alternating dark bands and light interbands. bands that are sites of gene expression expand to give chromosome paff (Balbiani rings).
Karnataka CET-2002
Principle of Inheritance and Variation
184687
Gynecomastia is a symptom of
1 Tumer's syndrome
2 Down's syndrome
3 Cri-du-chat syndrome
4 Klinefelter's syudrome
Explanation:
: Gynecomastia is a symptom of Klinefelters syndrome. The presence of 2 X chromosomes causes appearance of femine characters in male. It is triggered by a decreases in the amoum of the hormone testosterone compared with estrogen. - Gynecomastia is a condition where there will be an enlargement of the male breast. - Klinefelter's syntrome is chatacterized by trisomy (XXY). There are 47 chromosomes instead of nomal 46.
Kerala PMT-2008
Principle of Inheritance and Variation
184688
The affected male in the pedigree chart is symbolized by
1234
Show/Hide Explanation
Explanation:
: Shaded square represent the affected male in the pedigree chart. - A pedigree is a family tree or chart made of symbols and lines that represent a person's genetic family history. - In pedigree, symbol represent people and line tepresent genetic relationships.
Karnataka CET-2022
Principle of Inheritance and Variation
184690
Both sickle cell anaemia and Huntingtons chorea are
1 bacteria related diseases
2 congenital disorders
3 pollutant induced disorders
4 virus related diseases
Explanation:
: Both sickle cell anaemia and Huntington's chores are congerital disorder. Congerital disorders can defined as structural or functional abrormalities that occur during intrauterine life. It is also called birth defects. Fickle cell anaemia is autosome linked reccesive trait that can be transmitted from parents to offspring when both the parents are carrier for the gene. Huntington's chored an inherited condition in which nerve cells in the brain break down overtime.
BCECE-2014
Principle of Inheritance and Variation
184691
Absorption of tosic amounts of iron due to a genetically defective control mechanisms is known as
1 Haenatochromatosis
2 Haemosiderosis
3 Haemoptysis
4 Haematoma.
Explanation:
: Absorption of toxic amount of iron due to a gentically defective control mechamism is known as haematochromatosis. It is most common autosomal tecessive genetic disorder and the most common cause of severe iron overload. Hereditary, Haematochromatosis is a disorder that causes the body to absorb too much iron from the diet. The excess iron accumulate in and eventually damages the body tissue and organs.
184685
Balbiani rings are the structural features of:
1 allosomes
2 autosomes
3 lampbrush chromosomes
4 polytene chromosomes
Explanation:
: Balbiani rings are the structural feature of polytene chromosomes. - Polytene chromosomes were cliscovered by Balbiani in 1882 in larval salivary of Chironimus. - It is specialized interphase chromosomes present in certain insect cells. - Cells with polytene chromosomes undergo repeated rounds of DNA teplication without cell division. - Polytene chromosomes have alternating dark bands and light interbands. bands that are sites of gene expression expand to give chromosome paff (Balbiani rings).
Karnataka CET-2002
Principle of Inheritance and Variation
184687
Gynecomastia is a symptom of
1 Tumer's syndrome
2 Down's syndrome
3 Cri-du-chat syndrome
4 Klinefelter's syudrome
Explanation:
: Gynecomastia is a symptom of Klinefelters syndrome. The presence of 2 X chromosomes causes appearance of femine characters in male. It is triggered by a decreases in the amoum of the hormone testosterone compared with estrogen. - Gynecomastia is a condition where there will be an enlargement of the male breast. - Klinefelter's syntrome is chatacterized by trisomy (XXY). There are 47 chromosomes instead of nomal 46.
Kerala PMT-2008
Principle of Inheritance and Variation
184688
The affected male in the pedigree chart is symbolized by
1234
Show/Hide Explanation
Explanation:
: Shaded square represent the affected male in the pedigree chart. - A pedigree is a family tree or chart made of symbols and lines that represent a person's genetic family history. - In pedigree, symbol represent people and line tepresent genetic relationships.
Karnataka CET-2022
Principle of Inheritance and Variation
184690
Both sickle cell anaemia and Huntingtons chorea are
1 bacteria related diseases
2 congenital disorders
3 pollutant induced disorders
4 virus related diseases
Explanation:
: Both sickle cell anaemia and Huntington's chores are congerital disorder. Congerital disorders can defined as structural or functional abrormalities that occur during intrauterine life. It is also called birth defects. Fickle cell anaemia is autosome linked reccesive trait that can be transmitted from parents to offspring when both the parents are carrier for the gene. Huntington's chored an inherited condition in which nerve cells in the brain break down overtime.
BCECE-2014
Principle of Inheritance and Variation
184691
Absorption of tosic amounts of iron due to a genetically defective control mechanisms is known as
1 Haenatochromatosis
2 Haemosiderosis
3 Haemoptysis
4 Haematoma.
Explanation:
: Absorption of toxic amount of iron due to a gentically defective control mechamism is known as haematochromatosis. It is most common autosomal tecessive genetic disorder and the most common cause of severe iron overload. Hereditary, Haematochromatosis is a disorder that causes the body to absorb too much iron from the diet. The excess iron accumulate in and eventually damages the body tissue and organs.
Show/Hide Explanation
