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Journal of Medical Genetics|March 2, 1999
A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancerN J Froggatt, J Green, C Brassett, et al.Human Molecular Genetics|February 1, 1994
Somatic NF2 gene mutations in familial and non-familial vestibular schwannomaR M Irving, D A Moffat, D G Hardy, et al.Human Molecular Genetics|July 1, 1997
Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHLE R Woodward, C Eng, R McMahon, et al.Human Molecular Genetics|December 1, 1996
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathwayK W Brown, A J Villar, W Bickmore, et al.Cancer Research|April 5, 2005
Transcriptional regulation of cyclin A2 by RASSF1A through the enhanced binding of p120E4F to the cyclin A2 promoterJalal Ahmed-Choudhury, Angelo Agathanggelou, Sarah L Fenton, et al.Oncogene|February 19, 2013
Knockdown of Slingshot 2 (SSH2) serine phosphatase induces Caspase3 activation in human carcinoma cell lines with the loss of the Birt-Hogg-Dubé tumour suppressor gene (FLCN)X Lu, U Boora, L Seabra, et al.Fetal Diagnosis and Therapy|June 20, 2014
BAC chromosomal microarray for prenatal detection of chromosome anomalies in fetal ultrasound anomalies: an economic evaluationSarah C Hillman, Pelham M Barton, Tracy E Roberts, et al.Endocrine Research|October 21, 2014
A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defectHakan Cangul, Feyza Darendeliler, Yaman Saglam, et al.Optics Letters|June 15, 2017
Dual-axis optical coherence tomography for deep tissue imagingYang Zhao, Will J Eldridge, Jason R Maher, et al.JACC. Clinical Electrophysiology|July 22, 2023
Correlation Between Functional Substrate Mapping and Cardiac Computed Tomography-Derived Wall Thinning for Ventricular Tachycardia AblationTimothy R Maher, Benjamin L Freedman, Andrew H Locke, et al.Pageof 63