Cytogenetics of Fragile X Chromosome: Autosomal Sites as Potential Markers for Fragile X Chromosome Analysis
Author:
Affiliation:
1. Departments of Human Genetics and Psychiatry, Bangalore 560 029, Karnataka, India
2. National Institute of Mental Health and Neurosciences, Bangalore 560 029, Karnataka, India
Publisher
Kamla Raj Enterprises
Subject
Genetics (clinical),Genetics
Link
https://www.tandfonline.com/doi/pdf/10.1080/09723757.2001.11885740
Reference4 articles.
1. Manjunatha KR, Rao BSS, Narayanan HS, Girimaji SR, Shobha S, Gandhi DH, Sangvi R 1988. Fragile X syn-drome: The first case report from India.Genome,30(Suppl):205.
2. Russel O 1985.Mental Handicap, London: Churchill Livingstone.
3. Sutherland GR, Hecht F 1985.Fragile Sites on Human Chromosomes.Oxford Monographs on Medical Ge-netics. London: Oxford University Press.
4. Wang 0, Green E, Barnicoat A, Garrett D, Mullarkey M, Bobrow M, Mathew CG 1993. Cytogenetic versus DNA diagnosis in routine referrals for fragile X syn-drome.Lancet,3-42 (8878): 1025-1026.
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Cytogenetic Investigations in Mentally Challenged Individuals;International Journal of Human Genetics;2011-06
2. Genetics of Fragile X Syndrome: A Systematic Data from the Indian Population;International Journal of Human Genetics;2002-06
3. Frequency, Association and Genetic Implications of Chromosomal Fragile Sites in Mental Retardation;International Journal of Human Genetics;2002-03
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