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Victoria Murday

Showing results (1-10 of 21) with videos related to

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International Journal of Cardiology|December 10, 2015
A de-novo deletion of dystrophin provoking severe 'peri-partum cardiomyopathy': The importance of genetic testing in peripartum cardiomyopathy to uncover female carriersAyesha Ahmed, Stefan Spinty, Victoria Murday, et al.
Familial Cancer|May 8, 2004
An audit of screening for familial breast cancer before 50 years in the South Thames Region - have we got it right?Victoria Murday, R Pears, J Ball, et al.
International Journal of Cardiology|February 19, 2009
Andersen-Tawil syndromeRobin A P Weir, Colin J Petrie, Victoria Murday, et al.
Clinical Dysmorphology|August 25, 2010
Novel features in auriculo-condylar syndromeRuth McGowan, Victoria Murday, Esther Kinning, et al.
Heart Rhythm|May 13, 2014
Novel SCN5A mutation in amiodarone-responsive multifocal ventricular ectopy-associated cardiomyopathyThomas M Beckermann, Karen McLeod, Victoria Murday, et al.
European Journal of Medical Genetics|March 3, 2017
Long QT syndrome and left ventricular noncompaction in 4 family members across 2 generations with KCNQ1 mutationMira Kharbanda, Amanda Hunter, Stephen Tennant, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 29, 2011
Diagnostic use of skeletal survey in suspected skeletal dysplasiaAmith Kumar Iynapillai Veeramani, Paul Higgins, Sandra Butler, et al.
European Journal of Medical Genetics|August 6, 2011
Clinical features and respiratory complications in Myhre syndromeRuth McGowan, Ramkumar Gulati, Pamela McHenry, et al.
BMC Genomics|March 19, 2005
Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndromeNicholas C M Hearle, Ian Tomlinson, Wendy Lim, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new casesSahar Mansour, Fiona Connell, Colin Steward, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
International Journal of Cardiology|December 10, 2015
A de-novo deletion of dystrophin provoking severe 'peri-partum cardiomyopathy': The importance of genetic testing in peripartum cardiomyopathy to uncover female carriersAyesha Ahmed, Stefan Spinty, Victoria Murday, et al.
Familial Cancer|May 8, 2004
An audit of screening for familial breast cancer before 50 years in the South Thames Region - have we got it right?Victoria Murday, R Pears, J Ball, et al.
International Journal of Cardiology|February 19, 2009
Andersen-Tawil syndromeRobin A P Weir, Colin J Petrie, Victoria Murday, et al.
Clinical Dysmorphology|August 25, 2010
Novel features in auriculo-condylar syndromeRuth McGowan, Victoria Murday, Esther Kinning, et al.
Heart Rhythm|May 13, 2014
Novel SCN5A mutation in amiodarone-responsive multifocal ventricular ectopy-associated cardiomyopathyThomas M Beckermann, Karen McLeod, Victoria Murday, et al.
European Journal of Medical Genetics|March 3, 2017
Long QT syndrome and left ventricular noncompaction in 4 family members across 2 generations with KCNQ1 mutationMira Kharbanda, Amanda Hunter, Stephen Tennant, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 29, 2011
Diagnostic use of skeletal survey in suspected skeletal dysplasiaAmith Kumar Iynapillai Veeramani, Paul Higgins, Sandra Butler, et al.
European Journal of Medical Genetics|August 6, 2011
Clinical features and respiratory complications in Myhre syndromeRuth McGowan, Ramkumar Gulati, Pamela McHenry, et al.
BMC Genomics|March 19, 2005
Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndromeNicholas C M Hearle, Ian Tomlinson, Wendy Lim, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new casesSahar Mansour, Fiona Connell, Colin Steward, et al.
Pageof 3