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Match the column-I with column-II and re-write the matching pairs. Column-I1. 21 trisomy2. X-monosomy3. Holandric traits4. Feminized male - Biology

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प्रश्न

Match the column-I with column-II and re-write the matching pairs.

Column-I Column-II
1. 21 trisomy a. Turner’s syndrome
2. X-monosomy b. Klinefelter’s syndrome
3. Holandric traits c. Down's syndrome
4. Feminized male d. Hypertrichosis
जोड्या लावा/जोड्या जुळवा
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उत्तर

Column-I Column-II
1. 21 trisomy c. Down's syndrome
2. X-monosomy a. Turner’s syndrome
3. Holandric traits d. Hypertrichosis
4. Feminized male b. Klinefelter’s syndrome
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पाठ 3: Inheritance and Variation - Exercises [पृष्ठ ६९]

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बालभारती Biology [English] Standard 12 Maharashtra State Board
पाठ 3 Inheritance and Variation
Exercises | Q 4 | पृष्ठ ६९

व्हिडिओ ट्यूटोरियलVIEW ALL [2]

संबंधित प्रश्‍न

A child suffering from Thalassemia is born to a normal couple. But the mother is being blamed by the family for delivering a sick baby. 

  1. What is Thalassemia?
  2. How would you counsel the family not to blame the mother for delivering a child suffering from this disease? Explain.
  3. List the values your counselling can propagate in the families.

What do sex linked traits appear in males than in females? 


Read the following statements and select the correct option.

i. Genetic disorders are broadly categorised as, Mendelian disorders and chromosomal disorders.

ii. Mendelian disorders are caused due to absence or excess of one or more chromosomes or their abnormal arrangement.

iii. Chromosomal disorders are mainly caused due to alteration or mutation in the gene.


Match the Column I and Column II and select the correct option.

  List-I   List-II
i. Holandric genes a. Pleiotropy
ii. Multiple effects of a single gene b. Hypertrichosis
iii. Skin colour in man c. Multiple Alleles
iv. ABO Blood types d. Polygenic inheritance

The correct answer is


Choose the correct option which appropriately classifies the following disorders into Mendelian and chromosomal disorders:

Colour blindness, Down syndrome, Sickle cell anaemia, Turner syndrome, Thalassemia, Haemophilia, Phenylketonuria, Klinefelter syndrome.


Conditions of a karyotype 2n ± 1 and 2n ± 2 are called ______.


This abnormality occurs due to monosomy (2n - 1); the individual has 2n = 45 chromosomes with 44 + XO genotype.


Placed below is a karyotype of a human being.

On the basis of this karyotype, which of the following conclusions can be drawn: ______ 


The technique exployed in human genetic counselling is:


What are chromosomal disorders?


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