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Non-invasive prenatal diagnosis using fetal DNA in maternal plasma: a preliminary study for identification of paternally-inherited alleles using single nucleotide polymorphisms

BMJ open, 2015-07, Vol.5 (7), p.e007648-e007648

2015

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Characterisation of β-globin Gene Mutations in Malaysian Children: A Strategy for the Control of β-Thalassaemia in a Developing Country

Journal of tropical pediatrics (1980), 2005-12, Vol.51 (6), p.328-333

2005

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Rapid detection of α-thalassaemia variants using droplet digital PCR

International journal of laboratory hematology, 2016-08, Vol.38 (4), p.435-443

2016

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The use of Taqman genotyping assays for rapid confirmation of β-thalassaemia mutations in the Malays: accurate diagnosis with low DNA concentrations

International journal of laboratory hematology, 2015-02, Vol.37 (1), p.79-89

2015

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Specific and straightforward molecular investigation of β-thalassemia mutations in the Malaysian Malays and Chinese using direct TaqMan genotyping assays

Genetics and molecular research, 2013-01, Vol.12 (3), p.2409-2415

2013

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Chelation Therapy with Desferrioxamine does not Normalize Ferritin Level but Attenuates Oxidative Damage and Improves Total Antioxidant Level in Malaysian Chinese β-thalassaemia Major Patients

West Indian medical journal, 2011, Vol.60 (1), p.3-8

2011

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Paraoxonase 1 Status in Keratoconus: A Preliminary Study of Activity and Polymorphism

West Indian medical journal, 2012-09, Vol.61 (6), p.569-573

2012

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Alpha-Thalassaemia in Association with Beta-Thalassaemia Patients in Malaysia: A Study on the Co-Inheritance of Both Disorders

Community genetics, 2008-01, Vol.11 (3), p.129-134

2008

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Molecular defects in the beta-globin gene identified in different ethnic groups/populations during prenatal diagnosis for beta-thalassemia: a Malaysian experience

Clinical and experimental medicine, 2004-12, Vol.4 (3), p.142-147

2004

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Single versus multiple fractions of repeat radiation for painful bone metastases: a randomised, controlled, non-inferiority trial

The lancet oncology, 2014-02, Vol.15 (2), p.164-171

2014

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Analysis of α1 and α2 globin genes among patients with hemoglobin Adana in Malaysia

Genetics and molecular research, 2016-04, Vol.15 (2)

2016

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Analysis of alpha 1 and alpha 2 globin genes among patients with hemoglobin Adana in Malaysia

Genetics and molecular research, 2016-01, Vol.15 (2)

2016

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Screening for intermediate and severe forms of thalassaemia in discarded red blood cells: optimization and feasibility

Medical journal of Malaysia, 2011-12, Vol.66 (5), p.429-434

2011

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Population Genetic Study among the Orang Asli (Semai Senoi) of Malaysia: Malayan Aborigines

Human biology, 1995-02, Vol.67 (1), p.37-57

1995

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Effect of nonsolvent additive on the surface morphology and the gas separation performance of poly(2,6-dimethyl-1,4-phenylene)oxide membranes

Journal of membrane science, 1999-07, Vol.160 (1), p.7-16

1999

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Rapid and cost-effective antenatal diagnosis of haemoglobin Bart's hydrops foetalis syndrome using a duplex-polymerase chain reaction

Medical journal of Malaysia, 2005-10, Vol.60 (4), p.447-453

2005

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Screening of concurrent alpha-thalassaemia 1 in beta-thalassaemia carriers

Medical journal of Malaysia, 2006-06, Vol.61 (2), p.217-220

2006

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Sex-specific effects of nutritional supplements in infants born early or small: protocol for an individual participant data meta-analysis (ESSENCE IPD-MA)

BMJ open, 2020-01, Vol.10 (1), p.e033438-e033438

2020

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Prenatal diagnosis of α- and β-thalassaemias in Singapore-current status

Annals of tropical paediatrics, 1991-01, Vol.11 (1), p.67-74

1991

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The amplification refractory mutation system (ARMS): A rapid and direct prenatal diagnostic technique for β-thalassaemia in Singapore

Prenatal diagnosis, 1994-11, Vol.14 (11), p.1077-1082

1994

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Mutation analysis of the BRCAI gene in malaysian breast cancer patients

Singapore medical journal, 2002-04, Vol.43 (4), p.194-197

2002

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Mutation analysis of the BRCA1 gene in Malaysian breast cancer patients

Singapore medical journal, 2002-04, Vol.43 (4), p.194-197

2002

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Molecular defects in the [beta]-globin gene identified in different ethnic groups/populations during prenatal diagnosis for [beta]-thalassemia: a Malaysian experience

Clinical and experimental medicine, 2004-04, Vol.4 (3), p.142

2004

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The spectrum of β-thalassemia mutations in Malays in Singapore and Kelantan

Southeast Asian journal of tropical medicine and public health, 1996-03, Vol.27 (1), p.164-168

1996

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Molecular characterization of /3-thalassaemia in Singaporean Chinese: Application to prenatal diagnosis

Journal of paediatrics and child health, 1993-12, Vol.29 (6), p.461-463

1993

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Non-invasive prenatal diagnosis using fetal DNA in maternal plasma: a preliminary study for identification of paternally-inherited alleles using single nucleotide polymorphisms

Characterisation of β-globin Gene Mutations in Malaysian Children: A Strategy for the Control of β-Thalassaemia in a Developing Country

Rapid detection of α-thalassaemia variants using droplet digital PCR

The use of Taqman genotyping assays for rapid confirmation of β-thalassaemia mutations in the Malays: accurate diagnosis with low DNA concentrations

Specific and straightforward molecular investigation of β-thalassemia mutations in the Malaysian Malays and Chinese using direct TaqMan genotyping assays

Chelation Therapy with Desferrioxamine does not Normalize Ferritin Level but Attenuates Oxidative Damage and Improves Total Antioxidant Level in Malaysian Chinese β-thalassaemia Major Patients

Paraoxonase 1 Status in Keratoconus: A Preliminary Study of Activity and Polymorphism

Alpha-Thalassaemia in Association with Beta-Thalassaemia Patients in Malaysia: A Study on the Co-Inheritance of Both Disorders

Molecular defects in the beta-globin gene identified in different ethnic groups/populations during prenatal diagnosis for beta-thalassemia: a Malaysian experience

Single versus multiple fractions of repeat radiation for painful bone metastases: a randomised, controlled, non-inferiority trial

Analysis of α1 and α2 globin genes among patients with hemoglobin Adana in Malaysia

Analysis of alpha 1 and alpha 2 globin genes among patients with hemoglobin Adana in Malaysia

Screening for intermediate and severe forms of thalassaemia in discarded red blood cells: optimization and feasibility

Population Genetic Study among the Orang Asli (Semai Senoi) of Malaysia: Malayan Aborigines

Effect of nonsolvent additive on the surface morphology and the gas separation performance of poly(2,6-dimethyl-1,4-phenylene)oxide membranes

Rapid and cost-effective antenatal diagnosis of haemoglobin Bart's hydrops foetalis syndrome using a duplex-polymerase chain reaction

Screening of concurrent alpha-thalassaemia 1 in beta-thalassaemia carriers

Sex-specific effects of nutritional supplements in infants born early or small: protocol for an individual participant data meta-analysis (ESSENCE IPD-MA)

Prenatal diagnosis of α- and β-thalassaemias in Singapore-current status

The amplification refractory mutation system (ARMS): A rapid and direct prenatal diagnostic technique for β-thalassaemia in Singapore

Mutation analysis of the BRCAI gene in malaysian breast cancer patients

Mutation analysis of the BRCA1 gene in Malaysian breast cancer patients

Molecular defects in the [beta]-globin gene identified in different ethnic groups/populations during prenatal diagnosis for [beta]-thalassemia: a Malaysian experience

The spectrum of β-thalassemia mutations in Malays in Singapore and Kelantan

Molecular characterization of /3-thalassaemia in Singaporean Chinese: Application to prenatal diagnosis

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