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British Journal of Haematology|August 8, 1998
Prenatal diagnosis of Glanzmann thrombasthenia using the polymorphic markers BRCA1 and THRA1 on chromosome 17D L French, B S Coller, S Usher, et al.
Carcinogenesis|July 17, 1998
Comprehensive mutational scanning of the p53 coding region by two-dimensional gene scanningR D Rines, N J van Orsouw, I Sigalas, et al.
The Journal of Hospital Infection|April 13, 2011
Bacterial contamination of hands and the environment in a microbiology laboratoryL S Y Ng, W T Teh, S K Ng, et al.
The Journal of Clinical Endocrinology and Metabolism|January 3, 2001
Differential genetic alterations in von Hippel-Lindau syndrome-associated and sporadic pheochromocytomasB U Bender, M Gutsche, S Gläsker, et al.
Plant & Cell Physiology|May 16, 2017
The ARM Domain of ARMADILLO-REPEAT KINESIN 1 is Not Required for Microtubule Catastrophe But Can Negatively Regulate NIMA-RELATED KINASE 6 in Arabidopsis thalianaRyan C Eng, Laryssa S Halat, Samuel J Livingston, et al.
Human Pathology|March 7, 2001
Genomic alterations in tubular breast carcinomasF M Waldman, E S Hwang, J Etzell, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|December 7, 2011
Comparison of phenotypic methods and matrix-assisted laser desorption ionisation time-of-flight mass spectrometry for the identification of aero-tolerant Actinomyces spp. isolated from soft-tissue infectionsL S Y Ng, J H C Sim, L C Eng, et al.
The Journal of Biological Chemistry|October 17, 1998
Different classes of coactivators recognize distinct but overlapping binding sites on the estrogen receptor ligand binding domainF C Eng, A Barsalou, N Akutsu, et al.
Clinical Genetics|February 1, 1997
Mutation of RET codon 768 is associated with the FMTC phenotypeL M Boccia, J S Green, C Joyce, et al.
Oncogene|July 22, 1998
PTEN/MMAC1/TEP1 involvement in primary prostate cancersS Pesche, A Latil, F Muzeau, et al.
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