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D DeLozier

Showing results (31-40 of 41) with videos related to

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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.
Journal of Medical Genetics|February 1, 1996
The clinical, molecular, and pathological characterisation of a family with two cases of lethal perinatal type 2 Gaucher diseaseE Sidransky, N Tayebi, B K Stubblefield, 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.
Journal of Medical Genetics|April 10, 2009
Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesiaM Failly, L Bartoloni, A Letourneau, et al.
Cytogenetics and Cell Genetics|November 4, 2000
No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD)A K Maiti, L Bartoloni, H M Mitchison, et al.
Schweizerische Medizinische Wochenschrift|July 7, 1979
[Prenatal diagnosis. Review, personal and prospective studies]E Engel, J Empson, D DeLozier, 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.
Genomics|March 15, 2001
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesiaL Bartoloni, J L Blouin, A K Maiti, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
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.
Journal of Medical Genetics|February 1, 1996
The clinical, molecular, and pathological characterisation of a family with two cases of lethal perinatal type 2 Gaucher diseaseE Sidransky, N Tayebi, B K Stubblefield, 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.
Journal of Medical Genetics|April 10, 2009
Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesiaM Failly, L Bartoloni, A Letourneau, et al.
Cytogenetics and Cell Genetics|November 4, 2000
No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD)A K Maiti, L Bartoloni, H M Mitchison, et al.
Schweizerische Medizinische Wochenschrift|July 7, 1979
[Prenatal diagnosis. Review, personal and prospective studies]E Engel, J Empson, D DeLozier, 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.
Genomics|March 15, 2001
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesiaL Bartoloni, J L Blouin, A K Maiti, et al.
Pageof 5