Asian Journal of Nursing Education and Research

Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Karyotyping:Spying the Faulty Genes


Affiliations
1 Army College of Nursing, Jalandhar Cantt, India
     

   Subscribe/Renew Journal


Karyotype is number of chromosomes and its appearance in the nucleus of a eukaryotic cell3. And the study of karyotype is called Karyotyping or chromosomal analysis. It provides insight to the genes in order to detect any genetic and chromosomal problems. A small sample of individual’s cells is sufficient to rule out ischolar_main cause of genetic disorder. In this, chromosomes of an organism are paired and ordered by using standardised staining procedure, enables to analyze its characteristics and structural features2. It reveals chromosomal deletions, translocations, duplication and inversions2. Karyotyping in the present scenario indeed act as a boon and ensure wellbeing of foetus.

Keywords

Karyotype, Congenital Anomalies, Foetus, Genetic Mutations, Chromosome and Genes.
Subscription Login to verify subscription
User
Notifications
Font Size


  • https ://www.nature.com/scitable/topicpage/karyotyping-for-chromosomal-anormalities-298

  • https://www.labtestsonline.org.au/learning/test-index/chromosome-analysis-karyotyping

  • . https://en.wikipedia.org/wiki/Karyotype

  • . https://www.webmd.com/baby/what-is-a-karyotype-test#1

  • https://www.verywellhealth.com/how-to-how-is-a-karyotype-test-done-1120402

  • . https://www.lalpathlabs.com/blog/karyotype-test/


Abstract Views: 493

PDF Views: 0




  • Karyotyping:Spying the Faulty Genes

Abstract Views: 493  |  PDF Views: 0

Authors

Rashmi Sharma
Army College of Nursing, Jalandhar Cantt, India

Abstract


Karyotype is number of chromosomes and its appearance in the nucleus of a eukaryotic cell3. And the study of karyotype is called Karyotyping or chromosomal analysis. It provides insight to the genes in order to detect any genetic and chromosomal problems. A small sample of individual’s cells is sufficient to rule out ischolar_main cause of genetic disorder. In this, chromosomes of an organism are paired and ordered by using standardised staining procedure, enables to analyze its characteristics and structural features2. It reveals chromosomal deletions, translocations, duplication and inversions2. Karyotyping in the present scenario indeed act as a boon and ensure wellbeing of foetus.

Keywords


Karyotype, Congenital Anomalies, Foetus, Genetic Mutations, Chromosome and Genes.

References