Comprehensive cytogenetic analysis of cases referred for suspected chromosomal abnormalities: A Five-year study at Advanced Medical and Dental Institute (AMDI), Universiti Sains Malaysia, Penang, Malaysia.
Abstract
Keywords
Full Text:
PDFReferences
LG Shaffer, LJ Campbell, ML Slovak (2009). ISCN 2009: An International System for Human Cytogenetic Nomenclature. 1st ed. Karger: Basel; 2009.
RS Verma, H Dosik (1980). Incidence of major chromosomal abnormalities in a referred population for suspected chromosomal aberrations: a report of 357 cases. Clinical Genetics. [Online] 17, pp. 305-308.
WS Choi, KH Kim, YK Paik (1984). A cytogenetic study in patients referred for suspected chromosomal abnormalities. Journal of Hanyang Medical College. [Online] 4, pp. 565-597.
SS Kim, SC Jung, HJ Kim, HR Moon, JS Lee (1999). Chromosome abnormalities in a referred population of suspected chromosomal aberrations: a report of 4117 cases. Journal of Korean Medical Science. [Online] 14, pp. 373-376.
M Balkan, H Akbas, H Isi, D Oral, A Turkyilmaz, S Kalkanli, et al. (2010). Cytogenetic analysis of 4216 patients referred for suspected chromosomal abnormalities in Southeast Turkey. Genetics and Molecular Research. [Online] 9(2), pp. 1094-1103.
SN Heyn, D Perlstein, editors. Down Syndrome [monograph on the internet]. California: eMedicineHealth, WebMD; 2011 [cited 2011 Oct 10]. Available from: http://www.emedicinehealth.com/down_syndrome/article_em.htm/.
EB Hook, JL Hamerton (1977). The frequency of chromosome abnormalities detected in consecutive newborn studies, differences between studies, results by sex and by severity of phenotypic involvement. In: Hook EB, Porter IH, editors. Population cytogenetics: studies in humans. New York: Academic Press; [Online] pp. 63-79.
J Nielsen, M Wohlert (1991). Chromosome abnormalities found among 34910 newborn children: results from a 13-year incidence study in Arhus, Denmark. Human Genetics. [Online] 87, pp. 81-83.
Genetics Home Reference [homepage on the Internet]. Bethesda, MD: Trisomy 13, U.S. National Library of Medicine; c2009-11 [updated 2009 Jan; cited 2011 Oct 10]. Available from: http://ghr.nlm.nih.gov/condition/trisomy-13#definition/.
Genetics Home Reference [homepage on the Internet]. Bethesda, MD: Trisomy 18, U.S. National Library of Medicine; c2009-11 [updated 2009 Jan; cited 2011 Oct 10]. Available from: http://ghr.nlm.nih.gov/condition/trisomy-18#definition/.
Spalding J., Genetics Mosaics Support Group [monograph on the internet]. Laurel, MD: xyTurners; 2004 [cited 2011 Oct 10]. Available from: http://www.xyxo.org/index.html/.
[ National Institute of Child Health & Human Development [homepage on the Internet]. Bethesda, MD: U.S. National Institutes of Health; c2007-11 [updated 2007 May 24; cited 2011 Oct 10]. Available from: http://www.nichd.nih.gov/health/topics/klinefelter_syndrome.cfm/.
Genetics Home Reference [homepage on the Internet]. Bethesda, MD: Turner Syndrome, U.S. National Library of Medicine; c2008-11 [updated 2008 May; cited 2011 Oct 10]. Available from: http://ghr.nlm.nih.gov/condition/turner-syndrome#definition/.
JA Jewell, B Buehler, editors. Fragile X Syndrome [monograph on the internet]. California: Medscape Reference, WebMD; 2011 [cited 2011 Oct 10]. Available from: http://emedicine.medscape.com/article/943776-overview#a0101/.
Genetics Home Reference [homepage on the Internet]. Bethesda, MD: Fragile X Syndrome, U.S. National Library of Medicine; c2007-11 [updated 2007 May; cited 2011 Oct 10]. Available from: http://ghr.nlm.nih.gov/condition/fragile-x-syndrome#definition/.
FI Sahin, Z Yilmaz, OO Yuregir, T Bulakbasi, O Ozer, HB Zeyneloglu (2008). Chromosome heteromorphism an impact on infertility. J Assist Reprod Genet. [Online] 25, pp. 191–195.
AR Brothman, NR Schneider, I Saikevych, LD Cooley, MG Butler, S Patil, et al. (2006). Cytogenetic heteromorphisms: Survey results and reporting practices of Giemsa-band regions that we have pondered for years. Arch Pathol Lab Med. [Online] 130(7), pp. 947–949.
K Yakin, B Balaban, B Urman (2005). Is there a possible correlation between chromosomal variants and spermatogenesis?. International Journal of Urology. [Online] 12, pp. 984-989.
Copyright (c) 2017 Journal of Biomedical and Clinical Sciences (JBCS)
Copyright © 2016 AMDI Publisher, Universiti Sains Malaysia.
Disclaimer : This website has been updated to the best of our knowledge to be accurate. However, Universiti Sains Malaysia shall not be liable for any loss or damage caused by the usage of any information obtained from this web site.
Best viewed: Mozilla Firefox 4.0 & Google Chrome at 1024 × 768 resolution.