Homocysteine metabolism enzyme gene polymorphisms in non-syndromic Malaysian congenital heart disease patients
Congenital heart disease (CHD) mainly is caused by the incomplete development of the heart during the first 6 weeks of pregnancy. Chromosomal and genetic abnormalities in the child and high levels of homocysteine in the blood are some of the risk factors related to CHD. Several studies in various po...
Saved in:
Main Author: | Mohamad, Nur Afiqah |
---|---|
Format: | Thesis |
Language: | English |
Published: |
2013
|
Subjects: | |
Online Access: | http://psasir.upm.edu.my/id/eprint/75324/1/FPSK%28M%29%202013%2051%20IR.pdf |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Analysis of genetic polymorphisms of TBX5, NKX2-5 and GATA4 cardiac transcription factor genes in Malaysian non syndromic congenital heart disease subjects
by: Khadhim, Nora F.
Published: (2012) -
Analysis of Genetic Polymorphisms as Risk Factors in Essential Hypertension and Type 2 Diabetes Mellitus among Malaysians
by: Vasudevan, R.
Published: (2009) -
Analysis of genetic polymorphism as risk factor of diabetes nephropathy among type 2 diabetic patients of a tertiary hospital
by: Yahya, Mohd Jokha
Published: (2017) -
Polymorphism of Haemoglobin-e in Selected Malaysian and the Maldives Populations
by: Saleem, Mohamed
Published: (2011) -
Biochemical polymorphisms in goats with special reference to the Katjang goat /
by: Noor Hasima Nagoor Pitchai
Published: (1986)