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M A Morris

Showing results (51-60 of 152) with videos related to

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European Journal of Human Genetics : EJHG|December 22, 1999
The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene clusterM Neerman-Arbez, S E Antonarakis, A Honsberger, et al.
The Journal of Gene Medicine|February 6, 2002
N-acetylcysteine augments adenovirus-mediated gene expression in human endothelial cells by enhancing transgene transcription and virus entryL Jornot, M A Morris, H Petersen, et al.
The Journal of Clinical Investigation|January 23, 1999
Deletion of the fibrinogen [correction of fibrogen] alpha-chain gene (FGA) causes congenital afibrogenemiaM Neerman-Arbez, A Honsberger, S E Antonarakis, et al.
Journal De Genetique Humaine|January 1, 1989
[Chorionic villus sampling (CVS): level of activity and methods to resolve certain difficulties in interpretation]C D Delozier-Blanchet, P Extermann, M A Morris, et al.
Lancet (London, England)|June 14, 1997
The illness of Gerard Manley HopkinsF Biagi, H J Ellis, M A Morris, et al.
Journal of Pediatric Urology|June 27, 2019
Surgical decision-making in infants with suspected UPJ obstruction: stakeholder perspectivesV M Vemulakonda, M K Hamer, A Kempe, et al.
Clinical Genetics|May 20, 2003
Familial predisposition to tufted angioma: identification of blood and lymphatic vascular componentsJ C Tille, M A Morris, M A Bründler, et al.
The New England Journal of Medicine|April 1, 1982
Increased circulating Ia-antigen-bearing T cells in type I diabetes mellitusR A Jackson, M A Morris, B F Haynes, et al.
The Journal of Bone and Joint Surgery. British Volume|November 1, 1992
Lipids and Dupuytren's diseaseP L Sanderson, M A Morris, J K Stanley, et al.
Clinical Genetics|June 11, 1999
A proven case of materno-foetal transfusion determined by cytogenetic and DNA analysisA Paoloni-Giacobino, M H Dutoit, M A Morris, et al.
Pageof 16

Showing results (51-60 of 152) with videos related to

Sort By:
Pageof 16
European Journal of Human Genetics : EJHG|December 22, 1999
The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene clusterM Neerman-Arbez, S E Antonarakis, A Honsberger, et al.
The Journal of Gene Medicine|February 6, 2002
N-acetylcysteine augments adenovirus-mediated gene expression in human endothelial cells by enhancing transgene transcription and virus entryL Jornot, M A Morris, H Petersen, et al.
The Journal of Clinical Investigation|January 23, 1999
Deletion of the fibrinogen [correction of fibrogen] alpha-chain gene (FGA) causes congenital afibrogenemiaM Neerman-Arbez, A Honsberger, S E Antonarakis, et al.
Journal De Genetique Humaine|January 1, 1989
[Chorionic villus sampling (CVS): level of activity and methods to resolve certain difficulties in interpretation]C D Delozier-Blanchet, P Extermann, M A Morris, et al.
Lancet (London, England)|June 14, 1997
The illness of Gerard Manley HopkinsF Biagi, H J Ellis, M A Morris, et al.
Journal of Pediatric Urology|June 27, 2019
Surgical decision-making in infants with suspected UPJ obstruction: stakeholder perspectivesV M Vemulakonda, M K Hamer, A Kempe, et al.
Clinical Genetics|May 20, 2003
Familial predisposition to tufted angioma: identification of blood and lymphatic vascular componentsJ C Tille, M A Morris, M A Bründler, et al.
The New England Journal of Medicine|April 1, 1982
Increased circulating Ia-antigen-bearing T cells in type I diabetes mellitusR A Jackson, M A Morris, B F Haynes, et al.
The Journal of Bone and Joint Surgery. British Volume|November 1, 1992
Lipids and Dupuytren's diseaseP L Sanderson, M A Morris, J K Stanley, et al.
Clinical Genetics|June 11, 1999
A proven case of materno-foetal transfusion determined by cytogenetic and DNA analysisA Paoloni-Giacobino, M H Dutoit, M A Morris, et al.
Pageof 16