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123 results on '"Lim, Weng Khong"'

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101. Genomic landscapes of breast fibroepithelial tumors

102. Mutational landscapes of tongue carcinoma reveal recurrent mutations in genes of therapeutic and prognostic relevance

103. Abstract 3874: Mutational landscapes of oral tongue squamous cell carcinoma reveal recurrent mutations in genes of therapeutic and prognostic relevance

105. Abstract 5184: Distinct mutational patterns in liver fluke-related and non-infection-related bile duct cancers revealed by whole exome sequencing

106. Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma

107. Exome sequencing identifies distinct mutational patterns in liver fluke–related and non-infection-related bile duct cancers

108. Genome-Wide Mutational Signatures of Aristolochic Acid and Its Application as a Screening Tool

110. Identification of Genetic Variants in Progressive Supranuclear Palsy in Southeast Asia.

111. Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen

112. Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen

113. Variation in predicted COVID-19 risk among lemurs and lorises

114. Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen

115. Activity of a heptad of transcription factors is associated with stem cell programs and clinical outcome in acute myeloid leukemia.

116. Dilated aorta in CNOT3 -related neurodevelopmental disorder: 'expanding' the phenotype.

117. Transcriptomic convergence despite genomic divergence drive field cancerization in synchronous squamous tumors.

118. Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese Ancestry.

119. A novel intronic variant in ROBO3 associated with horizontal gaze palsy with progressive scoliosis: case report and literature review.

120. ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk.

121. The landscape of tolerated genetic variation in humans and primates.

122. Variation in predicted COVID-19 risk among lemurs and lorises.

123. Integrated paired-end enhancer profiling and whole-genome sequencing reveals recurrent CCNE1 and IGF2 enhancer hijacking in primary gastric adenocarcinoma.

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