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Familial Cancer|June 14, 2005
Screening for exonic copy number mutations at MSH2 and MLH1 by MAPHSeyed Mohammad Akrami, Malcolm G Dunlop, Susan M Farrington, et al.Journal of Medical Genetics|July 2, 2013
Comparison of the clinical scoring systems in Silver-Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testingRenuka P Dias, Peter Nightingale, Carol Hardy, et al.European Journal of Human Genetics : EJHG|January 26, 2017
Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosageMichael Parks, Samantha Court, Benjamin Bowns, et al.Clinical Epigenetics|July 2, 2014
Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjectsAbdulla Ibrahim, Gail Kirby, Carol Hardy, et al.American Journal of Medical Genetics. Part A|September 18, 2009
Microarray based analysis of 3p25-p26 deletions (3p- syndrome)Salwati Shuib, Dominic McMullan, Eleanor Rattenberry, et al.Clinical Epigenetics|December 12, 2013
Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technologyLouise Tee, Derek Hk Lim, Renuka P Dias, et al.Archives of Neurology|June 15, 2011
Neuropathy in a human without the PMP22 geneMario Andre Saporta, Istvan Katona, Xuebao Zhang, et al.F1000Research|March 18, 2014
Mutation detection in cholestatic patients using microarray resequencing of ATP8B1 and ABCB11Kirsten E McKay, Christopher K Bruce, Jane L Hartley, et al.Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|February 3, 2022
Vasomotor symptoms in early breast cancer-a "real world" exploration of the patient experienceKatherine Marie Cole, Mark Clemons, Mashari Alzahrani, et al.Human Reproduction (Oxford, England)|December 17, 2008
Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologiesDerek Lim, Sarah C Bowdin, Louise Tee, et al.Pageof 6