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Proceedings of the National Academy of Sciences of the United States of America|June 21, 1994
Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer familiesM Nyström-Lahti, P Sistonen, J P Mecklin, et al.
Thyroid : Official Journal of the American Thyroid Association|June 15, 2016
Primary Cell Culture Systems for Human Thyroid StudiesYanqiang Wang, Wei Li, John E Phay, et al.
Angewandte Chemie (International Ed. in English)|October 8, 2019
Towards Reliable and Quantitative Surface-Enhanced Raman Scattering (SERS): From Key Parameters to Good Analytical PracticeSteven E J Bell, Gaëlle Charron, Emiliano Cortés, et al.
Biomedical Optics Express|March 21, 2019
Label-free self-referenced sensing of living cells by terahertz metamaterial-based reflection spectroscopyXiang Zhao, Zhongquan Lin, Yunxia Wang, et al.
International Journal of Cancer|April 3, 1999
Cancer risk in mutation carriers of DNA-mismatch-repair genesM Aarnio, R Sankila, E Pukkala, et al.
International Journal of Cancer|March 4, 1997
Microsatellite instability in cervical and endometrial carcinomasA Helland, A L Børresen-Dale, P Peltomäki, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 1, 2004
Papillary and follicular thyroid carcinomas show distinctly different microarray expression profiles and can be distinguished by a minimum of five genesMicheala A Aldred, Ying Huang, Sandya Liyanarachchi, et al.
Cell|December 21, 1990
Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophiesJ Chelly, H Gilgenkrantz, M Lambert, et al.
Cancer Research|August 15, 1991
Evidence supporting exclusion of the DCC gene and a portion of chromosome 18q as the locus for susceptibility to hereditary nonpolyposis colorectal carcinoma in five kindredsP Peltomäki, P Sistonen, J P Mecklin, et al.
American Journal of Human Genetics|May 1, 1985
Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutationC Ingle, R Williamson, A de la Chapelle, et al.
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