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Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb].

Sindrom Fragile X merupakan salah satu penyakit pewarisan yang paling kerap menyebabkan keadaan kerencatan akal. Penyakit ini berlaku disebabkan oleh peningkatan jujukan trinukleotida ulangan (CGG) yang terletak dalam kawasan 5’ UTR gen FMR1 dan mengakibatkan perencatan fungsi gen ini. Fragile X...

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Main Author: Sidek, Mohamad Ros
Format: Thesis
Language:English
Published: 2006
Subjects:
RJ370-550 Diseases of children and adolescents
Online Access:http://eprints.usm.my/8366/1/ANALISIS_GENETIK_MOLEKUL_PESAKIT_SINDROM_FRAGILE_X_DI_HOSPITAL.pdf
http://eprints.usm.my/8366/
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spelling my.usm.eprints.8366 http://eprints.usm.my/8366/ Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb]. Sidek, Mohamad Ros RJ370-550 Diseases of children and adolescents Sindrom Fragile X merupakan salah satu penyakit pewarisan yang paling kerap menyebabkan keadaan kerencatan akal. Penyakit ini berlaku disebabkan oleh peningkatan jujukan trinukleotida ulangan (CGG) yang terletak dalam kawasan 5’ UTR gen FMR1 dan mengakibatkan perencatan fungsi gen ini. Fragile X syndrome is one of the most common inherited genetic disorders that cause mental retardation. This disease results from the expansion of a trinucleotide repeat (CGG)n sequences, located in the 5' UTR of FMR1 gene, that further inactivate the normal function of this gene. 2006 Thesis NonPeerReviewed application/pdf en http://eprints.usm.my/8366/1/ANALISIS_GENETIK_MOLEKUL_PESAKIT_SINDROM_FRAGILE_X_DI_HOSPITAL.pdf Sidek, Mohamad Ros (2006) Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb]. Masters thesis, Universiti Sains Malaysia.
institution Universiti Sains Malaysia
building Hamzah Sendut Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Sains Malaysia
content_source USM Institutional Repository
url_provider http://eprints.usm.my/
language English
topic RJ370-550 Diseases of children and adolescents
spellingShingle RJ370-550 Diseases of children and adolescents
Sidek, Mohamad Ros
Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb].
description Sindrom Fragile X merupakan salah satu penyakit pewarisan yang paling kerap menyebabkan keadaan kerencatan akal. Penyakit ini berlaku disebabkan oleh peningkatan jujukan trinukleotida ulangan (CGG) yang terletak dalam kawasan 5’ UTR gen FMR1 dan mengakibatkan perencatan fungsi gen ini. Fragile X syndrome is one of the most common inherited genetic disorders that cause mental retardation. This disease results from the expansion of a trinucleotide repeat (CGG)n sequences, located in the 5' UTR of FMR1 gene, that further inactivate the normal function of this gene.
format Thesis
author Sidek, Mohamad Ros
author_facet Sidek, Mohamad Ros
author_sort Sidek, Mohamad Ros
title Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb].
title_short Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb].
title_full Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb].
title_fullStr Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb].
title_full_unstemmed Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb].
title_sort analisis genetik molekul pesakit sindrom fragile x di hospital universiti sains malaysia (husm)[rj506.f73 r788 2006 f rb].
publishDate 2006
url http://eprints.usm.my/8366/1/ANALISIS_GENETIK_MOLEKUL_PESAKIT_SINDROM_FRAGILE_X_DI_HOSPITAL.pdf
http://eprints.usm.my/8366/
_version_ 1643700970695163904
score 13.15806

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