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Patrick J Morrison

Showing results (91-100 of 158) with videos related to

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Human Molecular Genetics|November 17, 2018
Association of prolactin receptor (PRLR) variants with prolactinomasCaroline M Gorvin, Paul J Newey, Angela Rogers, et al.
Nature Genetics|December 11, 2012
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, et al.
Cancer Research|November 17, 2005
BRCA1 and c-Myc associate to transcriptionally repress psoriasin, a DNA damage-inducible geneRichard D Kennedy, Julia J Gorski, Jennifer E Quinn, et al.
Clinical Endocrinology|May 2, 2024
Clinical management and outcome of head and neck paragangliomas (HNPGLs): A single centre retrospective studyMilad Darrat, Louis Lau, Colin Leonard, et al.
Annals of Clinical and Translational Neurology|December 15, 2021
Genetic defects are common in myopathies with tubular aggregatesQiang Gang, Conceição Bettencourt, Stefen Brady, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 30, 2005
TGFBR1*6A may contribute to hereditary colorectal cancerYansong Bian, Trinidad Caldes, Juul Wijnen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 3, 2017
Predictive testing of minors for Huntington's disease: The UK and Netherlands experiencesOliver W Quarrell, Angus J Clarke, Cecilia Compton, et al.
The Journal of Clinical Endocrinology and Metabolism|May 14, 2013
A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paragangliomaEleanor Rattenberry, Lindsey Vialard, Anna Yeung, et al.
The Journal of Clinical Endocrinology and Metabolism|October 31, 2013
Deletions of the PRKAR1A locus at 17q24.2-q24.3 in Carney complex: genotype-phenotype correlations and implications for genetic testingParaskevi Salpea, Anelia Horvath, Edra London, et al.
The New England Journal of Medicine|January 7, 2011
AIP mutation in pituitary adenomas in the 18th century and todayHarvinder S Chahal, Karen Stals, Martina Unterländer, et al.
Pageof 16

Showing results (91-100 of 158) with videos related to

Sort By:
Pageof 16
Human Molecular Genetics|November 17, 2018
Association of prolactin receptor (PRLR) variants with prolactinomasCaroline M Gorvin, Paul J Newey, Angela Rogers, et al.
Nature Genetics|December 11, 2012
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, et al.
Cancer Research|November 17, 2005
BRCA1 and c-Myc associate to transcriptionally repress psoriasin, a DNA damage-inducible geneRichard D Kennedy, Julia J Gorski, Jennifer E Quinn, et al.
Clinical Endocrinology|May 2, 2024
Clinical management and outcome of head and neck paragangliomas (HNPGLs): A single centre retrospective studyMilad Darrat, Louis Lau, Colin Leonard, et al.
Annals of Clinical and Translational Neurology|December 15, 2021
Genetic defects are common in myopathies with tubular aggregatesQiang Gang, Conceição Bettencourt, Stefen Brady, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 30, 2005
TGFBR1*6A may contribute to hereditary colorectal cancerYansong Bian, Trinidad Caldes, Juul Wijnen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 3, 2017
Predictive testing of minors for Huntington's disease: The UK and Netherlands experiencesOliver W Quarrell, Angus J Clarke, Cecilia Compton, et al.
The Journal of Clinical Endocrinology and Metabolism|May 14, 2013
A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paragangliomaEleanor Rattenberry, Lindsey Vialard, Anna Yeung, et al.
The Journal of Clinical Endocrinology and Metabolism|October 31, 2013
Deletions of the PRKAR1A locus at 17q24.2-q24.3 in Carney complex: genotype-phenotype correlations and implications for genetic testingParaskevi Salpea, Anelia Horvath, Edra London, et al.
The New England Journal of Medicine|January 7, 2011
AIP mutation in pituitary adenomas in the 18th century and todayHarvinder S Chahal, Karen Stals, Martina Unterländer, et al.
Pageof 16