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Sian Ellard

Showing results (21-30 of 439) with videos related to

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Human Mutation|August 20, 2013
Clinical applications of next-generation sequencing: the 2013 human genome variation society scientific meetingSian Ellard, George P Patrinos, William S Oetting
The Journal of Molecular Diagnostics : JMD|April 29, 2006
Rapid and sensitive real-time polymerase chain reaction method for detection and quantification of 3243A>G mitochondrial point mutationRinki Singh, Sian Ellard, Andrew Hattersley, et al.
Pediatric Diabetes|March 1, 2011
KCNJ11 activating mutations cause both transient and permanent neonatal diabetes mellitus in Cypriot patientsYiannis S Ioannou, Sian Ellard, Andrew Hattersley, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 13, 2010
Mutation surveyor: software for DNA sequence analysisJayne A L Minton, Sarah E Flanagan, Sian Ellard
Prenatal Diagnosis|July 18, 2003
Molecular genetic prenatal diagnosis for a case of autosomal recessive spondylocostal dysostosisNeil V Whittock, Peter D Turnpenny, Joep Tuerlings, et al.
Journal of Clinical Research in Pediatric Endocrinology|July 1, 2017
Pancreatic Agenesis due to Compound Heterozygosity for a Novel Enhancer and Truncating Mutation in the PTF1A GeneMonica Gabbay, Sian Ellard, Elisa De Franco, et al.
The Journal of Clinical Investigation|December 10, 2019
Prediction algorithms: pitfalls in interpreting genetic variants of autosomal dominant monogenic diabetesSian Ellard, Kevin Colclough, Kashyap A Patel, et al.
Indian Pediatrics|October 25, 2016
Hyperinsulinemic Hypoglycemia of Infancy due to Novel HADH Mutation in Two SiblingsAmit Kumar Satapathy, Vandana Jain, Sian Ellard, et al.
Diabetes Care|July 2, 2003
Etiological investigation of diabetes in young adults presenting with apparent type 2 diabetesKatharine R Owen, Amanda Stride, Sian Ellard, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|September 27, 2003
Response to treatment with rosiglitazone in familial partial lipodystrophy due to a mutation in the LMNA geneKatharine R Owen, Mollie Donohoe, Sian Ellard, et al.
Pageof 44

Showing results (21-30 of 439) with videos related to

Sort By:
Pageof 44
Human Mutation|August 20, 2013
Clinical applications of next-generation sequencing: the 2013 human genome variation society scientific meetingSian Ellard, George P Patrinos, William S Oetting
The Journal of Molecular Diagnostics : JMD|April 29, 2006
Rapid and sensitive real-time polymerase chain reaction method for detection and quantification of 3243A>G mitochondrial point mutationRinki Singh, Sian Ellard, Andrew Hattersley, et al.
Pediatric Diabetes|March 1, 2011
KCNJ11 activating mutations cause both transient and permanent neonatal diabetes mellitus in Cypriot patientsYiannis S Ioannou, Sian Ellard, Andrew Hattersley, et al.
Methods in Molecular Biology (Clifton, N.J.)|October 13, 2010
Mutation surveyor: software for DNA sequence analysisJayne A L Minton, Sarah E Flanagan, Sian Ellard
Prenatal Diagnosis|July 18, 2003
Molecular genetic prenatal diagnosis for a case of autosomal recessive spondylocostal dysostosisNeil V Whittock, Peter D Turnpenny, Joep Tuerlings, et al.
Journal of Clinical Research in Pediatric Endocrinology|July 1, 2017
Pancreatic Agenesis due to Compound Heterozygosity for a Novel Enhancer and Truncating Mutation in the PTF1A GeneMonica Gabbay, Sian Ellard, Elisa De Franco, et al.
The Journal of Clinical Investigation|December 10, 2019
Prediction algorithms: pitfalls in interpreting genetic variants of autosomal dominant monogenic diabetesSian Ellard, Kevin Colclough, Kashyap A Patel, et al.
Indian Pediatrics|October 25, 2016
Hyperinsulinemic Hypoglycemia of Infancy due to Novel HADH Mutation in Two SiblingsAmit Kumar Satapathy, Vandana Jain, Sian Ellard, et al.
Diabetes Care|July 2, 2003
Etiological investigation of diabetes in young adults presenting with apparent type 2 diabetesKatharine R Owen, Amanda Stride, Sian Ellard, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|September 27, 2003
Response to treatment with rosiglitazone in familial partial lipodystrophy due to a mutation in the LMNA geneKatharine R Owen, Mollie Donohoe, Sian Ellard, et al.
Pageof 44