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Celia D DeLozier

Showing results (1-10 of 6) with videos related to

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Clinical Neurology and Neurosurgery|May 2, 2017
A rare case of choroid plexus carcinoma that led to the diagnosis of Lynch syndrome (hereditary nonpolyposis colorectal cancer)Viola W Zhu, Sanjay Hinduja, Stevan R Knezevich, et al.
International Journal of Colorectal Disease|April 19, 2005
Double frameshift mutations in APC and MSH2 in the same individualClaudio Soravia, Celia D DeLozier, Zurana Dobbie, et al.
International Journal of Colorectal Disease|May 6, 2006
Double frameshift mutations in APC and MSH2 in the same individualClaudio Soravia, Celia D DeLozier, Zuzana Dobbie, et al.
Respiration; International Review of Thoracic Diseases|April 25, 2008
DNAI1 mutations explain only 2% of primary ciliary dykinesiaMike Failly, Alexandra Saitta, Analia Muñoz, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2002
Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesiaLucia Bartoloni, Jean-Louis Blouin, Yanzhen Pan, et al.
Human Molecular Genetics|June 23, 2007
Non-disjunction of chromosome 13Merete Bugge, Andrew Collins, Jens Michael Hertz, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Clinical Neurology and Neurosurgery|May 2, 2017
A rare case of choroid plexus carcinoma that led to the diagnosis of Lynch syndrome (hereditary nonpolyposis colorectal cancer)Viola W Zhu, Sanjay Hinduja, Stevan R Knezevich, et al.
International Journal of Colorectal Disease|April 19, 2005
Double frameshift mutations in APC and MSH2 in the same individualClaudio Soravia, Celia D DeLozier, Zurana Dobbie, et al.
International Journal of Colorectal Disease|May 6, 2006
Double frameshift mutations in APC and MSH2 in the same individualClaudio Soravia, Celia D DeLozier, Zuzana Dobbie, et al.
Respiration; International Review of Thoracic Diseases|April 25, 2008
DNAI1 mutations explain only 2% of primary ciliary dykinesiaMike Failly, Alexandra Saitta, Analia Muñoz, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2002
Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesiaLucia Bartoloni, Jean-Louis Blouin, Yanzhen Pan, et al.
Human Molecular Genetics|June 23, 2007
Non-disjunction of chromosome 13Merete Bugge, Andrew Collins, Jens Michael Hertz, et al.
Pageof 1