Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Patrick J Morrison

Showing results (61-70 of 158) with videos related to

Pageof 16
Sort By:
Springerplus|June 26, 2014
Familial urothelial cell carcinoma of the bladder with autosomal dominant inheritance and late onset phenotypeRobin Brown, Deirdre E Donnelly, Derek Allen, et al.
Springerplus|February 10, 2015
The prevalence of pica in tuberous sclerosis complexPatrick J Morrison, Tara O'Neill, Rachel Hardy, et al.
The British Journal of General Practice : the Journal of the Royal College of General Practitioners|May 2, 2020
A quick reference guide for rare disease: supporting rare disease management in general practiceAshleen Crowe, Helen McAneney, Patrick J Morrison, et al.
The Oncologist|June 19, 2012
Constellation of five facial features of tuberous sclerosis in a child with a TSC2 1808A>G mutationRachel Hardy, Charles W Shepherd, Deirdre E Donnelly, et al.
Digestive Diseases and Sciences|April 6, 2007
A splice-site mutation in exon 4 of the APC gene in a family with attenuated familial adenomatous polyposisSeamus J Murphy, Brian McIlhatton, W Peter Logan, et al.
The Ulster Medical Journal|March 29, 2020
Natural history of a fibrous cephalic plaque and sustained eight decade follow-up in an 80 year old with tuberous sclerosis complex type 2Claire W Kirk, Deirdre E Donnelly, Rachel Hardy, et al.
Familial Cancer|June 1, 2006
The RET mutation E768D confers a late-onset familial medullary thyroid carcinoma -- only phenotype with incomplete penetrance: implications for screening and management of carrier statusTabib Dabir, Steven J Hunter, Colin F J Russell, et al.
The Ulster Medical Journal|October 30, 2008
DiGeorge syndrome presenting as late onset hypocalcaemia in adulthoodPhilip C Johnston, Deirdre E Donnelly, Deirdre K Donnelly, et al.
Journal of Evaluation in Clinical Practice|March 24, 2007
Cancer genetics: consultants' perceptions of their roles, confidence and satisfaction with knowledgeSiobhan McCann, Domhnall MacAuley, Yvonne Barnett, et al.
Clinical Dysmorphology|April 16, 2019
Phenotypic delineation of a 12q21 deletion syndromeCaoimhe S McKenna, Nivedita Saxena, Tabib A Dabir, et al.
Pageof 16

Showing results (61-70 of 158) with videos related to

Sort By:
Pageof 16
Springerplus|June 26, 2014
Familial urothelial cell carcinoma of the bladder with autosomal dominant inheritance and late onset phenotypeRobin Brown, Deirdre E Donnelly, Derek Allen, et al.
Springerplus|February 10, 2015
The prevalence of pica in tuberous sclerosis complexPatrick J Morrison, Tara O'Neill, Rachel Hardy, et al.
The British Journal of General Practice : the Journal of the Royal College of General Practitioners|May 2, 2020
A quick reference guide for rare disease: supporting rare disease management in general practiceAshleen Crowe, Helen McAneney, Patrick J Morrison, et al.
The Oncologist|June 19, 2012
Constellation of five facial features of tuberous sclerosis in a child with a TSC2 1808A>G mutationRachel Hardy, Charles W Shepherd, Deirdre E Donnelly, et al.
Digestive Diseases and Sciences|April 6, 2007
A splice-site mutation in exon 4 of the APC gene in a family with attenuated familial adenomatous polyposisSeamus J Murphy, Brian McIlhatton, W Peter Logan, et al.
The Ulster Medical Journal|March 29, 2020
Natural history of a fibrous cephalic plaque and sustained eight decade follow-up in an 80 year old with tuberous sclerosis complex type 2Claire W Kirk, Deirdre E Donnelly, Rachel Hardy, et al.
Familial Cancer|June 1, 2006
The RET mutation E768D confers a late-onset familial medullary thyroid carcinoma -- only phenotype with incomplete penetrance: implications for screening and management of carrier statusTabib Dabir, Steven J Hunter, Colin F J Russell, et al.
The Ulster Medical Journal|October 30, 2008
DiGeorge syndrome presenting as late onset hypocalcaemia in adulthoodPhilip C Johnston, Deirdre E Donnelly, Deirdre K Donnelly, et al.
Journal of Evaluation in Clinical Practice|March 24, 2007
Cancer genetics: consultants' perceptions of their roles, confidence and satisfaction with knowledgeSiobhan McCann, Domhnall MacAuley, Yvonne Barnett, et al.
Clinical Dysmorphology|April 16, 2019
Phenotypic delineation of a 12q21 deletion syndromeCaoimhe S McKenna, Nivedita Saxena, Tabib A Dabir, et al.
Pageof 16