Search Results - "Ng, I. S."
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Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort
Published in Neurology (27-07-2004)“…Among 367 subjects, the authors analyzed 167 patients with essential tremor, sporadic progressive cerebellar ataxia, multiple-system atrophy, and atypical…”
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2
Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations
Published in Human genetics (01-11-2006)“…Isolated oral clefts, including cleft lip with/without cleft palate (CL/P) and cleft palate (CP), have a complex and heterogeneous etiology. Case-parent trios…”
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3
Genetic analysis of SCA2, 3 and 17 in idiopathic Parkinson's disease
Published in Neuroscience letters (31-07-2006)“…Recent reports of SCA2 and SCA3 patients who presented with levodopa responsive parkinsonism have generated considerable interest as they have implications for…”
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4
Expanded FMR1 alleles are rare in idiopathic Parkinson's disease
Published in Neurogenetics (01-02-2005)Get full text
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5
Robust fragile X (CGG)n genotype classification using a methylation specific triple PCR assay
Published in Journal of medical genetics (01-04-2004)Get full text
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6
MRI of carpal tunnel syndrome: before and after carpal tunnel release
Published in Clinical radiology (01-12-2021)“…Carpal tunnel syndrome (CTS) is the most common peripheral nerve entrapment syndrome. Magnetic resonance imaging (MRI) is increasingly used to diagnose CTS,…”
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7
DNA testing for fragile X syndrome in 255 males from special schools in Singapore
Published in Annals of the Academy of Medicine, Singapore (01-03-2000)“…Fragile X syndrome, the most common cause of inherited mental retardation, results from unstable expansion of a trinucleotide (CGG)n repeat in the FMR1 gene…”
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8
Novel germline BRCA1 mutations detected in women in Singapore who developed breast carcinoma before the age of 36 years
Published in Cancer (15-08-2000)“…BACKGROUND In recent years, although BRCA1 has been extensively investigated, the contribution of inherited BRCA1 mutations to breast carcinoma in Asian…”
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9
Del(3) (p25.3) without phenotypic effect
Published in Journal of medical genetics (01-12-1995)“…A terminal deletion of chromosome 3 at p25.3 was observed during prenatal diagnosis. A similar deletion is also present in the phenotypically normal mother…”
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10
Deletion of the terminal segment of the long arm of chromosome 4 with aortic stenosis
Published in Journal of paediatrics and child health (01-12-1993)“…A dysmorphic Chinese baby girl was found to have deletion of the long arm of chromosome 4 (46XX, del[4] q33-->qter). A review of various case reports of…”
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Huntington's disease: recent progress in gene mapping and potential local application in Singapore
Published in Annals of the Academy of Medicine, Singapore (01-05-1993)“…Advances in the field of molecular genetics have made testing of individuals for the presence of certain genes possible. Programmes for testing families with…”
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12
Chemical transformation of α-pinene-derived organosulfate via heterogeneous OH oxidation: implications for sources and environmental fates of atmospheric organosulfates
Published in Atmospheric chemistry and physics (29-04-2022)“…Organosulfur compounds are found to be ubiquitous in atmospheric aerosols – a majority of which are expected to be organosulfates (OSs). Given the atmospheric…”
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13
Huntington's disease in five siblings
Published in Annals of the Academy of Medicine, Singapore (01-05-1993)“…Huntington's disease is an autosomal dominant neurodegenerative condition which is rare in Singapore. Five siblings with progressive chorea and dementia were…”
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14
β-thalassemia mutations in Singapore : a strategy for prenatal diagnosis
Published in Human genetics (01-10-1994)“…The strategy for early prenatal diagnosis of beta-thalassemia in Singapore by direct detection of the mutant beta-globin gene requires the spectrum of…”
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15
Subtle translocation (18;21) confirmed by FISH in a patient with Down syndrome
Published in Clinical genetics (01-11-1996)“…The patient presented with the typical features of Down syndrome; hypotonia, brachycephaly, flattened occiput, bilateral prominent medical epicanthic folds,…”
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SMN1 deletions among singaporean patients with spinal muscular atrophy
Published in Annals of the Academy of Medicine, Singapore (01-01-2005)“…Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder characterised by degeneration of spinal cord anterior horn cells, leading to…”
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17
Investigation of lipases from various Carica papaya varieties for hydrolysis of olive oil and kinetic resolution of ( R, S)-profen 2,2,2-trifluoroethyl thioesters
Published in Process biochemistry (1991) (01-03-2006)“…With olive oil hydrolysis in aqueous solutions and hydrolytic resolution of ( R, S)-profen 2,2,2-trifluoroethyl thioesters in water-saturated isooctane as the…”
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18
Expanded FMR1 alleles are rare in idiopathic Parkinson?s disease
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19
The simultaneous presence of alpha- and beta-thalassaemia alleles: a pitfall of thalassaemia screening
Published in Community genetics (2003)“…To compare the efficacy of routine haematological tests and molecular analysis in the diagnosis of double heterozygous alpha- and beta-thalassaemia. Screening…”
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Partially purified Carica papaya lipase: a versatile biocatalyst for the hydrolytic resolution of (R,S)-2-arylpropionic thioesters in water-saturated organic solvents
Published in Biotechnology and bioengineering (05-07-2005)“…With the hydrolytic resolution of (R,S)‐naproxen 2,2,2‐trifluoroethyl thioesters in water‐saturated isooctane as a model system, improvements of the specific…”
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