Cytogenetic Investigations in Mentally Challenged Individuals
Author:
Affiliation:
1. Centre for Genetic Disorders, Guru Nanak Dev University, Amritsar 143 005, Punjab, India
Publisher
Kamla Raj Enterprises
Subject
Genetics (clinical),Genetics
Link
https://www.tandfonline.com/doi/pdf/10.1080/09723757.2011.11886129
Reference8 articles.
1. Benn PA, Perle MA 1992. Chromosome satining and banding techiques. In: DE Rooney, BH Czepulowski (Eds.):Human Cytogenetics. A Practical Approach. Volume I: New York: Oxford University Press, pp. 91-118.
2. Chetan GK, Latha P, Arathi R, Bhaskar Rao GV, Padma S, Venkatesh HN 2001. Cytogenetics of fragile X chromosome: Autosomal sites as potential markers for fragile X chromosome analysis.Int J Hum Genet, 1 (2): 91–95.
3. Chetan GK, Manjunatha KR, Arathi R, Latha P, Bhaskar Rao GV, Venkatesh HN 2002. Genetics of fragile X syndrome: A systematic data from the Indian population.Int J Hum Genet, 2 (2): 69–72.
4. Dave U, Shetty D 2010. Chromosomal abnormalities in mental retardation: Indian experience.Int J Hum Genet, 10(1-3): 21–32.
5. Decoufle P, Boyle CA, Paulozzi LJ, Lary JM 2001. Increased risk for developmental disabilities in children who have major birth defects: A population-based study.Pediatrics, 108 (3): 728–734.
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