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2015 | 07 |

Tytuł artykułu

Mapping of India’s contribution on “Down syndrome” during 40 years from 1973-2012

Autorzy

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Down syndrome, a genetic disease, is commonly diagnosed congenital malformation/mental retardation syndrome occurring in people of all races and economic levels. The present study is aimed to examine the contribution of Indian scientists on Down syndrome during the 40 years span from 1973-2012. The study analyses the Indian share in the research output, contribution and citation impact of top Indian institutions, most prolific Indian authors, top journals for publication, top collaborating countries, number of citations received and the highly cited papers in the Indian research on Down syndrome.

Wydawca

-

Rocznik

Tom

07

Opis fizyczny

p.21-33,fig.,ref.

Twórcy

autor
  • Department of Library and Information Science, Maharshi Dayanand University, Rohtak, Haryana, India

Bibliografia

  • [1] Brook J.D., Gosden R.G., Chandley A.C. Maternal ageing and aneuploid embryos-- evidence from the mouse that biological and not chronological age is the important influence. Human Genetics 66 (1) (1984) 41-45.
  • [2] Deccan Herald News Service. Down syndrome still fatal in India. Deccan Herald, April 19, 2013.
  • [3] Ghosh S., Feingold E., Chakraborty S., Dey S.K. Telomere length is associated with types of chromosome 21 nondisjunction: a new insight into the maternal age effect on Down Syndrome birth. Human Genetics, 127(4) (2010) 403-409.
  • [4] Jones, K. L. Recognizable patterns of human malformation. Philadelphia: Elsevier (2006).
  • [5] NDSS - National Down Syndrome Society. What Is Down Syndrome? Retrieved from www.ndss.org/Down-Syndrome/What-Is-Down-Syndrome/
  • [6] Penrose, L.S. The relative effect of paternal and maternal age in Mongolism. Journal of Genetics, 27(2) (1933) 219-224.
  • [7] Penrose, L.S. The relative etiological importance of birth order and maternal age in Mongolism. Proceedings of the Royal Society B Biological Sciences, 115 (1934) 431-450.
  • [8] Powell-Hamilton, Nina N. Down Syndrome (Trisomy 21; Trisomy G). In Merck Manual Home Health Handbook for Patients and Caregivers. Retrieved from www.merckmanuals.com/home/childrens_health_issues/chromosomal_and_genetic_abnormalities/down_syndrome_trisomy_21_trisomy_g.html?qt=&sc=&alt=
  • [9] Verma, I.C. Personal communication. As cited in Jayalakshamma et al. Cytogenetic Analysis in Down Syndrome. International Journal of Human Genetics, 10(1-3) (2010) 95-99.
  • [10] WHO Genomic Resource Centre. Gene and human disease. Retrieved from http://www.who.int/genomics/public/geneticdiseases/en/index1.html#

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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