A Study Of The Genetic Variations In N-Terminus, C-Terminus And Promoter Of Rb1 Gene Among Retinoblastoma Patients In Malaysia

Retinoblastoma (RB) is the most common primary intraocular tumor affecting mainly children under five years of age, with a prevalence of 1 in 15 000 to 20 000 live births. Retinoblastoma is divided into hereditary and sporadic types. It is caused by mutations or changes in RB1 gene, a tumor suppress...

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Main Author: Hashim, Siti Norulhuda Haji Draman @
Format: Thesis
Language:English
Published: 2012
Subjects:
Online Access:http://eprints.usm.my/44906/1/SITI%20NORULHUDA%20BT%20HAJI%20DRAMAN%20%40%20HASHIM.pdf
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author Hashim, Siti Norulhuda Haji Draman @
author_facet Hashim, Siti Norulhuda Haji Draman @
author_sort Hashim, Siti Norulhuda Haji Draman @
collection USM
description Retinoblastoma (RB) is the most common primary intraocular tumor affecting mainly children under five years of age, with a prevalence of 1 in 15 000 to 20 000 live births. Retinoblastoma is divided into hereditary and sporadic types. It is caused by mutations or changes in RB1 gene, a tumor suppressor gene. The aim of this study is to detect mutations in N-terminus, C-terminus and promoter region of RB1 gene in retinoblastoma patients in Malaysia, as well as its association with staging and laterality of the patients. A total of 68 children with sporadic RB from Hospital Universiti Sains Malaysia (HUSM), Hospital Kuala Lumpur (HKL) and University Malaya Medical Centre (UMMC) and 68 healthy ethnic-matched controls were recruited.
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spelling usm.eprints-449062019-07-09T01:17:17Z http://eprints.usm.my/44906/ A Study Of The Genetic Variations In N-Terminus, C-Terminus And Promoter Of Rb1 Gene Among Retinoblastoma Patients In Malaysia Hashim, Siti Norulhuda Haji Draman @ R5-920 Medicine (General) Retinoblastoma (RB) is the most common primary intraocular tumor affecting mainly children under five years of age, with a prevalence of 1 in 15 000 to 20 000 live births. Retinoblastoma is divided into hereditary and sporadic types. It is caused by mutations or changes in RB1 gene, a tumor suppressor gene. The aim of this study is to detect mutations in N-terminus, C-terminus and promoter region of RB1 gene in retinoblastoma patients in Malaysia, as well as its association with staging and laterality of the patients. A total of 68 children with sporadic RB from Hospital Universiti Sains Malaysia (HUSM), Hospital Kuala Lumpur (HKL) and University Malaya Medical Centre (UMMC) and 68 healthy ethnic-matched controls were recruited. 2012-05 Thesis NonPeerReviewed application/pdf en http://eprints.usm.my/44906/1/SITI%20NORULHUDA%20BT%20HAJI%20DRAMAN%20%40%20HASHIM.pdf Hashim, Siti Norulhuda Haji Draman @ (2012) A Study Of The Genetic Variations In N-Terminus, C-Terminus And Promoter Of Rb1 Gene Among Retinoblastoma Patients In Malaysia. Masters thesis, Universiti Sains Malaysia.
spellingShingle R5-920 Medicine (General)
Hashim, Siti Norulhuda Haji Draman @
A Study Of The Genetic Variations In N-Terminus, C-Terminus And Promoter Of Rb1 Gene Among Retinoblastoma Patients In Malaysia
title A Study Of The Genetic Variations In N-Terminus, C-Terminus And Promoter Of Rb1 Gene Among Retinoblastoma Patients In Malaysia
title_full A Study Of The Genetic Variations In N-Terminus, C-Terminus And Promoter Of Rb1 Gene Among Retinoblastoma Patients In Malaysia
title_fullStr A Study Of The Genetic Variations In N-Terminus, C-Terminus And Promoter Of Rb1 Gene Among Retinoblastoma Patients In Malaysia
title_full_unstemmed A Study Of The Genetic Variations In N-Terminus, C-Terminus And Promoter Of Rb1 Gene Among Retinoblastoma Patients In Malaysia
title_short A Study Of The Genetic Variations In N-Terminus, C-Terminus And Promoter Of Rb1 Gene Among Retinoblastoma Patients In Malaysia
title_sort study of the genetic variations in n terminus c terminus and promoter of rb1 gene among retinoblastoma patients in malaysia
topic R5-920 Medicine (General)
url http://eprints.usm.my/44906/1/SITI%20NORULHUDA%20BT%20HAJI%20DRAMAN%20%40%20HASHIM.pdf
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