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Patrick J Morrison

Showing results (81-90 of 158) with videos related to

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Epilepsia|November 22, 2012
Recurrence risk of congenital malformations in infants exposed to antiepileptic drugs in uteroEllen Campbell, Emma Devenney, Jim Morrow, et al.
Neurology|January 11, 2013
Levetiracetam in pregnancy: results from the UK and Ireland epilepsy and pregnancy registersEllen Mawhinney, John Craig, Jim Morrow, et al.
European Journal of Human Genetics : EJHG|March 17, 2005
Genetic professionals' reports of nondisclosure of genetic risk information within familiesAngus Clarke, Martin Richards, Lauren Kerzin-Storrar, et al.
The Journal of Clinical Endocrinology and Metabolism|January 16, 2014
Clinical experience in the screening and management of a large kindred with familial isolated pituitary adenoma due to an aryl hydrocarbon receptor interacting protein (AIP) mutationFred Williams, Steven Hunter, Lisa Bradley, et al.
Journal of Neurology|October 31, 2012
The frequency of spinocerebellar ataxia type 23 in a UK populationKatherine Fawcett, Mohadeseh Mehrabian, Yo-Tsen Liu, et al.
The Journal of Clinical Endocrinology and Metabolism|July 9, 2014
Germline FH mutations presenting with pheochromocytomaGraeme R Clark, Marco Sciacovelli, Edoardo Gaude, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2018
Changing antiepilepsy drug-prescribing trends in women with epilepsy in the UK and Ireland and the impact on major congenital malformationsMichael O Kinney, James Morrow, Chris C Patterson, et al.
The Journal of Pathology. Clinical Research|February 6, 2020
Multifocal breast cancers are more prevalent in BRCA2 versus BRCA1 mutation carriersAlan D McCrorie, Susannah Ashfield, Aislinn Begley, et al.
Genes, Chromosomes & Cancer|January 17, 2020
Characterization of renal cell carcinoma-associated constitutional chromosome abnormalities by genome sequencingPhilip S Smith, James Whitworth, Hannah West, 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.
Pageof 16

Showing results (81-90 of 158) with videos related to

Sort By:
Pageof 16
Epilepsia|November 22, 2012
Recurrence risk of congenital malformations in infants exposed to antiepileptic drugs in uteroEllen Campbell, Emma Devenney, Jim Morrow, et al.
Neurology|January 11, 2013
Levetiracetam in pregnancy: results from the UK and Ireland epilepsy and pregnancy registersEllen Mawhinney, John Craig, Jim Morrow, et al.
European Journal of Human Genetics : EJHG|March 17, 2005
Genetic professionals' reports of nondisclosure of genetic risk information within familiesAngus Clarke, Martin Richards, Lauren Kerzin-Storrar, et al.
The Journal of Clinical Endocrinology and Metabolism|January 16, 2014
Clinical experience in the screening and management of a large kindred with familial isolated pituitary adenoma due to an aryl hydrocarbon receptor interacting protein (AIP) mutationFred Williams, Steven Hunter, Lisa Bradley, et al.
Journal of Neurology|October 31, 2012
The frequency of spinocerebellar ataxia type 23 in a UK populationKatherine Fawcett, Mohadeseh Mehrabian, Yo-Tsen Liu, et al.
The Journal of Clinical Endocrinology and Metabolism|July 9, 2014
Germline FH mutations presenting with pheochromocytomaGraeme R Clark, Marco Sciacovelli, Edoardo Gaude, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2018
Changing antiepilepsy drug-prescribing trends in women with epilepsy in the UK and Ireland and the impact on major congenital malformationsMichael O Kinney, James Morrow, Chris C Patterson, et al.
The Journal of Pathology. Clinical Research|February 6, 2020
Multifocal breast cancers are more prevalent in BRCA2 versus BRCA1 mutation carriersAlan D McCrorie, Susannah Ashfield, Aislinn Begley, et al.
Genes, Chromosomes & Cancer|January 17, 2020
Characterization of renal cell carcinoma-associated constitutional chromosome abnormalities by genome sequencingPhilip S Smith, James Whitworth, Hannah West, 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.
Pageof 16