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I Winship

Showing results (11-20 of 37) with videos related to

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Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 11, 2011
Neurosurgical considerations in von Hippel-Lindau diseaseM M Beitner, I Winship, K J Drummond
Journal of Genetic Counseling|August 31, 2013
Predictive genetic testing of a bone marrow recipient-ethical issues involving unexpected results, gender issues, test accuracy, and implications for the donorA Sexton, L Rawlings, M Jenkins, et al.
Internal Medicine Journal|April 23, 2014
Hereditary haemorrhagic telangiectasia, an Australian cohort: clinical and investigative featuresM Salaria, J Taylor, M Bogwitz, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Profound childhood deafness in southern AfricaP Beighton, D Viljoen, I Winship, et al.
Familial Cancer|December 29, 2010
Case report: renal cell carcinoma segregating with a t(2;3)(q37.3;q13.2) chromosomal translocation in an Ashkenazi Jewish familyL McKay, M Frydenberg, L Lipton, et al.
Internal Medicine Journal|March 18, 2010
Hereditary renal cell carcinoma: the clue can be in the skinM Harris, J Wallace, I Winship, et al.
Journal of Genetic Counseling|September 2, 2015
A Novel von Hippel Lindau Gene Intronic Variant and Its Reclassification from VUS to Pathogenic: the Impact on a Large FamilyA Sexton, L Rawlings, G McKavanagh, et al.
Human Molecular Genetics|January 1, 1994
A splice junction mutation in PAX3 causes Waardenburg syndrome in a South African familyJ Butt, J Greenberg, I Winship, et al.
Clinical Genetics|May 1, 1991
Piebaldism: an autonomous autosomal dominant entityI Winship, K Young, R Martell, et al.
Clinical Genetics|January 8, 2008
Cultural enhancement of a clinical service to meet the needs of indigenous people; genetic service development in response to issues for New Zealand MaoriR V Port, J Arnold, D Kerr, et al.
Pageof 4

Showing results (11-20 of 37) with videos related to

Sort By:
Pageof 4
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|January 11, 2011
Neurosurgical considerations in von Hippel-Lindau diseaseM M Beitner, I Winship, K J Drummond
Journal of Genetic Counseling|August 31, 2013
Predictive genetic testing of a bone marrow recipient-ethical issues involving unexpected results, gender issues, test accuracy, and implications for the donorA Sexton, L Rawlings, M Jenkins, et al.
Internal Medicine Journal|April 23, 2014
Hereditary haemorrhagic telangiectasia, an Australian cohort: clinical and investigative featuresM Salaria, J Taylor, M Bogwitz, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Profound childhood deafness in southern AfricaP Beighton, D Viljoen, I Winship, et al.
Familial Cancer|December 29, 2010
Case report: renal cell carcinoma segregating with a t(2;3)(q37.3;q13.2) chromosomal translocation in an Ashkenazi Jewish familyL McKay, M Frydenberg, L Lipton, et al.
Internal Medicine Journal|March 18, 2010
Hereditary renal cell carcinoma: the clue can be in the skinM Harris, J Wallace, I Winship, et al.
Journal of Genetic Counseling|September 2, 2015
A Novel von Hippel Lindau Gene Intronic Variant and Its Reclassification from VUS to Pathogenic: the Impact on a Large FamilyA Sexton, L Rawlings, G McKavanagh, et al.
Human Molecular Genetics|January 1, 1994
A splice junction mutation in PAX3 causes Waardenburg syndrome in a South African familyJ Butt, J Greenberg, I Winship, et al.
Clinical Genetics|May 1, 1991
Piebaldism: an autonomous autosomal dominant entityI Winship, K Young, R Martell, et al.
Clinical Genetics|January 8, 2008
Cultural enhancement of a clinical service to meet the needs of indigenous people; genetic service development in response to issues for New Zealand MaoriR V Port, J Arnold, D Kerr, et al.
Pageof 4