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Familial Cancer|December 22, 2011
Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutationsA Moran, C O'Hara, S Khan, et al.Clinical Genetics|December 1, 1995
Molecular genetic analysis of exons 1 to 6 of the APC gene in non-polyposis familial colorectal cancerJ A Joyce, N J Froggatt, R Davies, et al.Human Molecular Genetics|December 3, 2003
An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotypeAdele Murrell, Sarah Heeson, Wendy N Cooper, et al.Journal of Medical Genetics|February 5, 2022
Cost-effectiveness model of renal cell carcinoma (RCC) surveillance in hereditary leiomyomatosis and renal cell carcinoma (HLRCC)Alexander J Thompson, Yousef M Alwan, Vijay A C Ramani, et al.Human Molecular Genetics|September 1, 1997
Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndromeJ A Joyce, W K Lam, D J Catchpoole, et al.Journal of Neurosurgery|May 1, 1996
Molecular genetic investigation of the neurofibromatosis type 2 tumor suppressor gene in sporadic meningiomaT Harada, R M Irving, J H Xuereb, et al.Human Molecular Genetics|January 31, 2014
Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasoundKeren J Carss, Sarah C Hillman, Vijaya Parthiban, et al.EMBO Molecular Medicine|February 27, 2019
OTULIN deficiency in ORAS causes cell type-specific LUBAC degradation, dysregulated TNF signalling and cell deathRune Busk Damgaard, Paul R Elliott, Kirby N Swatek, et al.The Quarterly Journal of Medicine|September 1, 1989
Prognosis of critically-ill patients with acute renal failure: APACHE II score and other predictive factorsE R Maher, K N Robinson, J E Scoble, et al.The Journal of Clinical Endocrinology and Metabolism|March 1, 1996
Isolated familial pheochromocytoma as a variant of von Hippel-Lindau diseaseM M Ritter, A Frilling, P A Crossey, et al.Pageof 63