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Gastroenterology|August 9, 2005
Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1Tiina E Raevaara, Mari K Korhonen, Hannes Lohi, et al.
Thyroid : Official Journal of the American Thyroid Association|January 19, 2019
Risk Haplotypes Uniquely Associated with Radioiodine-Refractory Thyroid Cancer Patients of High African AncestryZachary Hurst, Sandya Liyanarachchi, Huiling He, et al.
Gastroenterology|July 8, 2008
The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutationsLeigha Senter, Mark Clendenning, Kaisa Sotamaa, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 30, 2005
TGFBR1*6A may contribute to hereditary colorectal cancerYansong Bian, Trinidad Caldes, Juul Wijnen, et al.
Gastroenterology|September 7, 2011
Variants in the netrin-1 receptor UNC5C prevent apoptosis and increase risk of familial colorectal cancerMarie-May Coissieux, Jerneja Tomsic, Marie Castets, et al.
The Journal of Frailty & Aging|March 25, 2026
Associations between frailty, biomarkers of cerebral pathology, cognitive and neuropsychiatric symptoms: a memory clinic studyVictor Gilles, Anthime Flaus, Achille Teillac, et al.
Leukemia|June 7, 2018
NF1 mutations are recurrent in adult acute myeloid leukemia and confer poor outcomeAnn-Kathrin Eisfeld, Jessica Kohlschmidt, Krzysztof Mrózek, et al.
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