about
Population genetic structure of peninsular Malaysia Malay sub-ethnic groupsClinical manifestations in trisomy 9Mapping human genetic diversity in AsiaAnalysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia.Permissibility of prenatal diagnosis and abortion for fetuses with severe genetic disorder: type 1 spinal muscular atrophyTowards understanding the low prevalence of Helicobacter pylori in Malays: genetic variants among Helicobacter pylori-negative ethnic Malays in the north-eastern region of Peninsular Malaysia and Han Chinese and South Indians.Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy.The first Malay database toward the ethnic-specific target molecular variation.Allele-specific PCR for a cost-effective & time-efficient diagnostic screening of spinal muscular atrophy.Contribution of 6p24 to non-syndromic cleft lip and palate in a Malay population: association of variants in OFC1Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studiesHarmonizing the interpretation of genetic variants across the world: the Malaysian experience.Dissecting the genetic structure and admixture of four geographical Malay populations.A whole genome analyses of genetic variants in two Kelantan Malay individualsGastric precancerous lesions are associated with gene variants in Helicobacter pylori-susceptible ethnic Malays.Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies.Novel complex re-arrangement of ARG1 commonly shared by unrelated patients with hyperargininemia.RB pocket domain B mutation frequency in Malaysia.Human Variome Project country nodes: documenting genetic information within a country.Mutation spectrum of dystrophin gene in malaysian patients with Duchenne/Becker muscular dystrophy.The population genomic landscape of human genetic structure, admixture history and local adaptation in Peninsular Malaysia.Screening for gap junction protein beta-2 gene mutations in Malays with autosomal recessive, non-syndromic hearing loss, using denaturing high performance liquid chromatography.Molecular description of familial defective APOB-100 in Malaysia.Maternal uniparental heterodisomy of chromosome 6 in a boy with an isolated cleft lip and palate.An improved rapid genotyping method for the study of beta-2 adrenergic receptor gene polymorphisms using single tube allele specific multiplex PCR.Genetic polymorphism of CYP2D6 in patients with cardiovascular disease -- a cohort study.A simple and rapid genotyping method for beta-2 receptor (beta2 AR) gene using allele specific multiplex PCR.Deletion analyses of SMN1 and NAIP genes in Malaysian spinal muscular atrophy patientsTransforming growth factor-alpha and nonsyndromic cleft lip with or without palate or cleft palate only in Kelantan, MalaysiaA polymorphic mutation, c.-3279T>G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the Malay populationDeletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophyDe novo interstitial deletion of 1q32.2-q32.3 including the entire IRF6 gene in a patient with oral cleft and other dysmorphic featuresPrevalence and molecular study of G6PD deficiency in Malaysian Orang AsliTwo closely spaced nonsense mutations in the DMD gene in a Malaysian familyContribution of variants in and near the IRF6 gene to the risk of nonsyndromic cleft lip with or without cleft palate in a Malay population
P50
Q21135497-155DBFAC-DC3B-45F3-9847-8955F3B8ACF7Q28109504-55FE0F19-6C0B-4CA7-B555-3F74D3E5E7D6Q28267585-202C3AF0-EB98-435D-8E4B-B67C6CCC00C0Q33850303-FFE064E1-BA18-4DAA-8CB5-CE23DDDDAA66Q34363145-01F11F82-82BA-4ACD-9D37-7C6B59520598Q34513377-F9ABCF10-264E-4AAB-AD04-1892F4188C80Q34848282-44A03C6D-5C8C-455A-A25B-5BE0281EB99EQ35633532-0F73C182-CFAB-4042-89B0-ED961D461130Q35838659-FD371A32-2F95-4EF3-97D4-03582B55E5F5Q35866596-4B6B1EA5-CDEF-4704-99DF-EDDEEE9D1451Q35871595-9398D24B-69D3-4224-BEBA-FA6E64E42FB9Q35936017-6FE9466E-ADC2-4412-92D4-7526DD6A2B73Q36099605-6D461CC9-EA6D-419E-AD31-5B4C73062EC5Q36387654-2AEF2993-1FFE-4C4A-A173-A08CC97CE86CQ36950918-5542F884-CAA0-453B-AF40-BF80838AFF99Q41688378-233BD427-F200-4504-AE4B-0C95748A0007Q42622129-5FBC53D1-2A34-4D01-BC40-F8B03B70A6C1Q43011222-F2FE2285-3915-468A-AAA3-05B5076CBB94Q45207504-2B65B2E3-7A14-48CC-ABDB-686434A73E12Q46085199-DF62E62E-CC81-4150-BF5A-AA6F3607BD70Q46487450-6841567A-DAB5-4610-A860-5405721CEFEAQ50452694-551EDAF0-FDB4-4496-9E93-DF605EA46C7AQ50899557-E6137798-5C00-420B-A2BB-95853E63F473Q53316216-6E060D1E-96C4-4170-870F-718937AF0ED7Q54566651-94D76F5A-6A69-4CA6-9DCC-28191A3DD9B3Q54690365-4E2B349B-4EB3-4B31-A339-364F64809E53Q54732036-3B8434E8-17FE-4661-B5D3-13D652E19116Q79651587-CFA81897-B632-4DBE-B4C3-1B606B7839B4Q79715157-10186E54-87A2-42EC-8F52-5B0CFF190006Q82433345-4A220266-AF0F-4823-A8F4-50655EDC7429Q83454561-540CF57F-FD53-4B04-9E84-F55E3089179CQ83743918-BDFE0EA7-51A8-4C15-88A1-C3CFDF3742CEQ83911724-17208EC6-FC6A-48A8-A2F9-85BCE6334FBBQ83938891-98F0ECD8-FD80-45F9-929A-FCA1376BCCB8Q84745218-0A26C7A2-9BE9-4C4C-B6F4-08B41099ED12
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Bin Alwi Zilfalil
@ast
Bin Alwi Zilfalil
@en
Bin Alwi Zilfalil
@es
Bin Alwi Zilfalil
@nl
Bin Alwi Zilfalil
@sl
type
label
Bin Alwi Zilfalil
@ast
Bin Alwi Zilfalil
@en
Bin Alwi Zilfalil
@es
Bin Alwi Zilfalil
@nl
Bin Alwi Zilfalil
@sl
prefLabel
Bin Alwi Zilfalil
@ast
Bin Alwi Zilfalil
@en
Bin Alwi Zilfalil
@es
Bin Alwi Zilfalil
@nl
Bin Alwi Zilfalil
@sl
P106
P1153
6507377118
P31
P496
0000-0001-5055-7892