A. S. Tan

发表

Spinocerebellar ataxia type 2 with focal epilepsy--an unusual association.

S. Chong, N. Tan, Y. Zhou, 2004, Annals of the Academy of Medicine, Singapore.

Simplified Preimplantation Genetic Diagnosis of Common Determinants of Hemoglobin Bart ’ s Hydrops Fetalis Syndrome Using a Multiplex-Microsatellite PCR Assay

Prasath, S. Loh, M. Choolani, 2012 .

Simplified PGD of common determinants of haemoglobin Bart's hydrops fetalis syndrome using multiplex-microsatellite PCR.

S. Loh, M. Choolani, S. Chong, 2010, Reproductive biomedicine online.

Rapid carrier screening for beta-thalassemia by single-step allele-specific PCR and detection.

S. Chong, H. Law, A. S. Tan, 2007, Clinical biochemistry.

Identification of Novel Microsatellite Markers Flanking the SMN1 and SMN2 Duplicated Region and Inclusion Into a Single-Tube Tridecaplex Panel for Haplotype-Based Preimplantation Genetic Testing of Spinal Muscular Atrophy

A. Agarwal, S. Chong, A. S. Tan, 2019, Front. Genet..

A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for alpha-thalassemia.

P. Low, S. Chong, A. S. Tan, 2001, Blood.

Single‐tube tetradecaplex panel of highly polymorphic microsatellite markers < 1 Mb from F8 for simplified preimplantation genetic diagnosis of hemophilia A

P. Wong, A. S. Tan, J. Mathew, 2017, Journal of thrombosis and haemostasis : JTH.

Hemoglobin H disease classification by isoelectric focusing: molecular verification of 110 cases from Thailand.

S. Chong, P. Sutcharitchan, A. S. Tan, 2005, Clinical chemistry.

Evidence of differential selection for the −α3.7 and −α4.2 single‐α‐globin gene deletions within the same population

A. S. Tan, S. Chong, Zhi Min Yap, 2013, European journal of haematology.

Single‐tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome

P. Wong, H. Law, A. S. Tan, 2015, Prenatal diagnosis.

Successful preimplantation genetic diagnosis of Hb Bart's hydrops fetalis in Singapore after fresh and frozen embryo replacement cycles.

S. Chong, A. S. Tan, Wen Wang, 2009, Annals of the Academy of Medicine, Singapore.

First successful preimplantation genetic diagnosis in Singapore--avoidance of beta-thalassaemia major.

S. Chong, A. S. Tan, Wen Wang, 2009, Annals of the Academy of Medicine, Singapore.

Preimplantation genetic diagnosis of chromosome translocations by analysis of polymorphic short tandem repeats.

S. Loh, M. Choolani, S. Chong, 2012, Singapore medical journal.

Identification of novel microsatellite markers <1 Mb from the HBB gene and development of a single‐tube pentadecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of beta‐thalassemia

A. S. Tan, S. Chong, F. S. H. Cheah, 2015, Electrophoresis.

Rapid and reliable preimplantation genetic diagnosis of common hemoglobin Bart's hydrops fetalis syndrome and hemoglobin H disease determinants using an enhanced single‐tube decaplex polymerase chain reaction assay

S. Loh, S. Ng, P. Wong, 2015, American journal of hematology.

Clinical report: a case of Williams Syndrome and Klinefelter Syndrome.

S. Chong, J. Lum, D. Goh, 2006, Annals of the Academy of Medicine, Singapore.

Molecular strategies for pre-implantation genetic diagnosis of single gene and chromosomal disorders.

S. Chong, A. S. Tan, B. Jiang, 2012, Best practice & research. Clinical obstetrics & gynaecology.

FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome

S. Loh, S. Chong, A. S. Tan, 2017, Expert Reviews in Molecular Medicine.

FMR 1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome

S. Loh, S. Chong, A. S. Tan, 2017 .

Third-Generation Single-Molecule Sequencing for Preimplantation Genetic Testing of Aneuploidy and Segmental Imbalances.

C. Khor, M. Choolani, A. S. Tan, 2023, Clinical chemistry.