S. Tan

发表

S. Tan, G. Kumar, S. K. Surrun, 2007, Travel medicine and infectious disease.

Sudden infant death in a tropical environment: Singapore's experience.

G. Lau, S. Tan, 1996, Forensic science international.

Human Fc gamma receptor IIA (FcγRIIA) genotyping and association with systemic lupus erythematosus (SLE) in Chinese and Malays in Malaysia

M. Phipps, SY. Tan, S. Tan, 1999, Lupus.

Clinical, radiological and serum amyloid P component scintigraphic features of beta2-microglobulin amyloidosis associated with continuous ambulatory peritoneal dialysis.

K. Farrington, M. Pepys, P. Hawkins, 1999, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Molecular mechanisms of fibrillogenesis and the protective role of amyloid P component: two possible avenues for therapy.

S. Radford, D. Booth, C. Robinson, 1996, Ciba Foundation symposium.

PCR-RFLP Genotyping of C1q Mutations and Single Nucleotide Polymorphisms in Malaysian Patients with Systemic Lupus Erythematosus

K. Chua, S. Tan, C. Chew, 2008, Human biology.

A study of association of the complement C4 mutations with systemic lupus erythematosus in the Malaysian population

SY. Tan, S. Tan, C. Chew, 2007, Lupus.

Bronchioloalveolar carcinoma with metastasis to the pituitary gland: a case report.

W. Poh, G. Lau, S. Tan, 1998, Journal of clinical pathology.

A distinct expression of CC chemokines by macrophages in nasopharyngeal carcinoma: implication for the intense tumor infiltration by T lymphocytes and macrophages.

K. Tang, S. Tan, S. Chan, 2001, Human pathology.

A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosis.

D. Booth, D. Vigushin, G. Tennent, 1995, QJM : monthly journal of the Association of Physicians.

An algorithmic approach to the diagnosis of NK and T cell lymphomas

K. Soo, S. Tan, L. Tan, 2011, Pathology.

A novel variant of transthyretin, 59Thr-->Lys, associated with autosomal dominant cardiac amyloidosis in an Italian family.

D. Booth, M. Pepys, P. Hawkins, 1995, Circulation.

Long term effect of renal transplantation on dialysis-related amyloid deposits and symptomatology.

M. Pepys, P. Hawkins, C. Winearls, 1996, Kidney international.

Primary localised amyloidosis of the orbit.

A. Garner, M. Pepys, P. Hawkins, 1996, The British journal of ophthalmology.

IDENTIFICATION OF MULTIPLE GENITAL HPV TYPES AND SEQUENCE VARIANTS BY CONSENSUS AND NESTED TYPE‐SPECIFIC PCR COUPLED WITH CYCLE SEQUENCING

V. Chow, E. Loh, V. Chow, 2000, Pathology.

The hereditary renal amyloidoses

S. Tan, 1999, Clinical and Experimental Nephrology.

Treatment of amyloidosis.

M. Pepys, P. Hawkins, S. Tan, 1995, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene.

D. Booth, M. Pepys, P. Hawkins, 1996, The Journal of clinical investigation.

Primary Localized Orbital Amyloidosis Composed of the Immunoglobulin γ Heavy Chain CH3 Domain

M. Pepys, P. Hawkins, J. Hsuan, 1994 .

Duplication of 8p with minimal phenotypic effect transmitted from a mother to her two daughters

J. Barber, S. Tan, B. Gibbons, 1999, Journal of medical genetics.

Association of clinicopathological features of melanoma with total naevus count and a history of dysplastic naevi: a cross‐sectional retrospective study within an academic centre

S. J. Lee, S. Tan, L. Strazzulla, 2018, Clinical and experimental dermatology.

Interstitial deletion of chromosome 5 in a neonate due to maternal insertion, ins(8;5)(p23;q33q35).

S. Tan, B. Gibbons, S. T. Lim, 1999, American journal of medical genetics.

Bilineal T lymphoblastic and myeloid blast transformation in chronic myeloid leukemia with TP53 mutation-an uncommon presentation in adults.

C. Chuah, S. Tan, S. Krishnan, 2013, Current oncology.

Pathohistogenetic approach on the etiology of Yunnan tin miner's lung cancer.

S. Tan, Z. You, S. Sun, 1989, Chinese Medical Journal.

Rapid prenatal diagnosis of chromosome abnormalities.

S. Tan, W. Chan, R. Quaife, 2000, Singapore medical journal.

Leiomyomatosis in an Infant With a SUFU Splice Site Variant: Case Report

R. Rao, M. McGuinness, S. Tan, 2022, Journal of pediatric hematology/oncology.

Intestinal Failure in Junctional Epidermolysis Bullosa: Mild Skin Disease, Severe Diarrhea

S. Tan, M. Pepper, S. Namjoshi, 2022, Digestive Diseases and Sciences.