Zobrazeno 1 - 10
of 22
pro vyhledávání: '"J. S. H. Tay"'
Publikováno v:
Royal Society Open Science, Vol 9, Iss 12 (2022)
High-quality lexical representations depend on robust representations of written form (orthography), spoken form (phonology) and meaning (semantics), and strong bonds between them. Quality of lexical representations may be affected by amount of print
Externí odkaz:
https://doaj.org/article/b70600f444704219b891d698712fc5e2
Publikováno v:
Journal of Paediatrics and Child Health. 29:461-463
Sixth-five 14-thalassaemia genes from 14 unrelated Chinese β-thalassaemia major patients and 37 Chinese β-carriers were analysed by allele-specific oligonucleotide (ASO) hybridization after DNA amplification by the polymerase chain reaction (PGR).
Publikováno v:
Acta Paediatrica. 85:1476-1482
In multiracial Singapore, the prevalence of coronary artery disease is highest in ethnic Indian and lowest in ethnic Chinese populations. Since susceptibility to coronary artery disease is closely associated with plasma lipid traits, we studied the c
Publikováno v:
Genetic Epidemiology. 9:1-10
The frequency of restriction fragment length polymorphisms (RFLPs) of the apolipoprotein B (apo B) gene, detected by XbaI and EcoRI, and their influence on serum lipids and apolipoproteins were studied in healthy Chinese of both sexes in Singapore. A
Publikováno v:
Japanese Journal of Human Genetics. 36:307-312
Biochemical characteristics of one non-deficient fast G6PD variant (GdSingapore) and six different deficient variants (three new, two Mahidol, one each of Indonesian and Mediterranean) were studied among the Malays of Singapore. The GdSingapore varia
Publikováno v:
Japanese journal of human genetics. 35:253-256
Three populations (Poliya, Deshi, and Tiyor) of the Koch ethnic group have been studied for the distribution of three serum protein and four red cell enzyme polymorphisms. There was no significant difference in the allelic frequencies of these system
Publikováno v:
Journal of Paediatrics and Child Health. 28:291-293
Rapid advances in the molecular genetics of Duchenne muscular dystrophy (DMD) and the discovery and localization of the gene product dystrophin has brought new hope that successful treatment for this disease may not be too far away. Dystrophin has be
Autor:
J. S. H. Tay
Publikováno v:
Journal of paediatrics and child health. 31(5)
Wilms' tumour, or nephroblastoma, is an embryonal malignancy of the kidney with an incidence of approximately 1 in 10,000 live births. It occurs in both sporadic and familial forms, but only 1% of Wilms' tumour patients have a positive family history
Autor:
Liang-In Lin, J. S. H. Tay, H. B. Wong, Norkamar Bt. Adb. Aziz, T. M. Chin, J. N. Chia, Shirley Kow Yin Kham, J. A. M. A. Tan
Publikováno v:
Prenatal diagnosis. 14(11)
beta-Thalassaemia major patients have chronic anaemia and since 3-4 per cent of Singaporeans carry the beta-gene, prenatal diagnosis is essential. We evaluated the amplification refractory mutation system (ARMS) technique as a routine test for prenat
Publikováno v:
Psychiatric genetics. 4(4)
Dopamine receptors have been implicated in the aetiology of schizophrenia and mode of action of antipsychotic drugs. A finding of increased homozygosity at the D3 receptor gene (BalI locus) has recently been reported. We have investigated the distrib