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Patrick J Morrison

Showing results (51-60 of 158) with videos related to

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Cerebellum (London, England)|November 14, 2019
Infantile Onset of Spinocerebellar Ataxia Type 5 (SCA-5) in a 6 Month Old with Ataxic Cerebral PalsyGillian Rea, Sandya Tirupathi, Jonathan Williams, et al.
European Journal of Medical Genetics|March 11, 2010
Delineation of a recognisable phenotype of interstitial deletion 3 (q22.3q25.1) in a case with previously unreported truncus arteriosusGillian Rea, Simon McCullough, Susan McNerlan, et al.
Archives of Disease in Childhood. Education and Practice Edition|June 23, 2026
Neonate with 'rocker-bottom' feet: what to do when it is not Edwards syndromePatrick J Morrison, Carl Harris, Ciaran Mccarthy, et al.
Diabetes Care|February 24, 2018
Zygodactyly (Syndactyly Type A1) Associated With Midfoot Charcot Neuropathy and DiabetesDominic O McConville, G Pooler Archbold, Anthony Lewis, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
A supernumerary chromosome 20, identified by FISH, in a male with azoospermia-cause or coincidence?S E McNerlan, Patrick J Morrison, N McClure, et al.
The Ulster Medical Journal|February 14, 2008
Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohortsLisa A Devlin, Colin A Graham, John H Price, et al.
The Ulster Medical Journal|March 28, 2018
Dystrophin Exon 29 Nonsense Mutations Cause a Variably Mild PhenotypeRebecca S Moore, Sandya Tirupathi, Brian Herron, et al.
The Oncologist|May 21, 2010
Advances in the genetics of familial renal cancerPatrick J Morrison, Deirdre E Donnelly, A Brew Atkinson, et al.
The Oncologist|September 22, 2011
Familial pediatric endocrine tumorsSarinda Millar, Lisa Bradley, Deirdre E Donnelly, et al.
BMJ Case Reports|June 19, 2012
Familial multiple lipomatosis with clear autosomal dominant inheritance and onset in early adolescenceCheng-Hiang Lee, Roy A J Spence, Meena Upadhyaya, et al.
Pageof 16

Showing results (51-60 of 158) with videos related to

Sort By:
Pageof 16
Cerebellum (London, England)|November 14, 2019
Infantile Onset of Spinocerebellar Ataxia Type 5 (SCA-5) in a 6 Month Old with Ataxic Cerebral PalsyGillian Rea, Sandya Tirupathi, Jonathan Williams, et al.
European Journal of Medical Genetics|March 11, 2010
Delineation of a recognisable phenotype of interstitial deletion 3 (q22.3q25.1) in a case with previously unreported truncus arteriosusGillian Rea, Simon McCullough, Susan McNerlan, et al.
Archives of Disease in Childhood. Education and Practice Edition|June 23, 2026
Neonate with 'rocker-bottom' feet: what to do when it is not Edwards syndromePatrick J Morrison, Carl Harris, Ciaran Mccarthy, et al.
Diabetes Care|February 24, 2018
Zygodactyly (Syndactyly Type A1) Associated With Midfoot Charcot Neuropathy and DiabetesDominic O McConville, G Pooler Archbold, Anthony Lewis, et al.
American Journal of Medical Genetics. Part A|February 5, 2003
A supernumerary chromosome 20, identified by FISH, in a male with azoospermia-cause or coincidence?S E McNerlan, Patrick J Morrison, N McClure, et al.
The Ulster Medical Journal|February 14, 2008
Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohortsLisa A Devlin, Colin A Graham, John H Price, et al.
The Ulster Medical Journal|March 28, 2018
Dystrophin Exon 29 Nonsense Mutations Cause a Variably Mild PhenotypeRebecca S Moore, Sandya Tirupathi, Brian Herron, et al.
The Oncologist|May 21, 2010
Advances in the genetics of familial renal cancerPatrick J Morrison, Deirdre E Donnelly, A Brew Atkinson, et al.
The Oncologist|September 22, 2011
Familial pediatric endocrine tumorsSarinda Millar, Lisa Bradley, Deirdre E Donnelly, et al.
BMJ Case Reports|June 19, 2012
Familial multiple lipomatosis with clear autosomal dominant inheritance and onset in early adolescenceCheng-Hiang Lee, Roy A J Spence, Meena Upadhyaya, et al.
Pageof 16