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Clinical Genetics
|
May 1, 1997
Linkage studies exclude the AT-V gene(s) from the translocation breakpoints in an AT-V patient
K Chrzanowska, M Stumm, M Bialecka, et al.
Human Molecular Genetics
|
April 1, 1995
Identification of Btk mutations in 20 unrelated patients with X-linked agammaglobulinaemia (XLA)
H Jin, A D Webster, M Vihinen, et al.
American Journal of Human Genetics
|
July 1, 1996
Ataxia-telangiectasia: mutations in ATM cDNA detected by protein-truncation screening
M Telatar, Z Wang, N Udar, et al.
Annals of Human Genetics
|
November 4, 2005
ATM gene founder haplotypes and associated mutations in Polish families with ataxia-telangiectasia
M Mitui, E Bernatowska, B Pietrucha, et al.
American Journal of Human Genetics
|
May 20, 1999
Splicing defects in the ataxia-telangiectasia gene, ATM: underlying mutations and consequences
S N Teraoka, M Telatar, S Becker-Catania, et al.
Molecular Genetics and Metabolism
|
June 30, 2000
Ataxia-telangiectasia: phenotype/genotype studies of ATM protein expression, mutations, and radiosensitivity
S G Becker-Catania, G Chen, M J Hwang, et al.
Clinical Immunology (Orlando, Fla.)
|
June 28, 2011
Efficacy and safety of Hizentra(®) in patients with primary immunodeficiency after a dose-equivalent switch from intravenous or subcutaneous replacement therapy
S Jolles, E Bernatowska, J de Gracia, et al.
Transplantation Proceedings
|
December 21, 2010
Liver transplantation for severe hepatic graft-versus-host disease in two children after hematopoietic stem cell transplantation
M Teisseyre, J Teisseyre, P Kalicinski, et al.
American Journal of Human Genetics
|
March 7, 1998
Ataxia-telangiectasia: identification and detection of founder-effect mutations in the ATM gene in ethnic populations
M Telatar, S Teraoka, Z Wang, et al.
Blood
|
January 11, 2000
Four novel mutations in the gene encoding gp91-phox of human NADPH oxidase: consequences for oxidase assembly
J H Leusen, C Meischl, M H Eppink, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 30) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 30 results.
Clinical Genetics
|
May 1, 1997
Linkage studies exclude the AT-V gene(s) from the translocation breakpoints in an AT-V patient
K Chrzanowska, M Stumm, M Bialecka, et al.
Human Molecular Genetics
|
April 1, 1995
Identification of Btk mutations in 20 unrelated patients with X-linked agammaglobulinaemia (XLA)
H Jin, A D Webster, M Vihinen, et al.
American Journal of Human Genetics
|
July 1, 1996
Ataxia-telangiectasia: mutations in ATM cDNA detected by protein-truncation screening
M Telatar, Z Wang, N Udar, et al.
Annals of Human Genetics
|
November 4, 2005
ATM gene founder haplotypes and associated mutations in Polish families with ataxia-telangiectasia
M Mitui, E Bernatowska, B Pietrucha, et al.
American Journal of Human Genetics
|
May 20, 1999
Splicing defects in the ataxia-telangiectasia gene, ATM: underlying mutations and consequences
S N Teraoka, M Telatar, S Becker-Catania, et al.
Molecular Genetics and Metabolism
|
June 30, 2000
Ataxia-telangiectasia: phenotype/genotype studies of ATM protein expression, mutations, and radiosensitivity
S G Becker-Catania, G Chen, M J Hwang, et al.
Clinical Immunology (Orlando, Fla.)
|
June 28, 2011
Efficacy and safety of Hizentra(®) in patients with primary immunodeficiency after a dose-equivalent switch from intravenous or subcutaneous replacement therapy
S Jolles, E Bernatowska, J de Gracia, et al.
Transplantation Proceedings
|
December 21, 2010
Liver transplantation for severe hepatic graft-versus-host disease in two children after hematopoietic stem cell transplantation
M Teisseyre, J Teisseyre, P Kalicinski, et al.
American Journal of Human Genetics
|
March 7, 1998
Ataxia-telangiectasia: identification and detection of founder-effect mutations in the ATM gene in ethnic populations
M Telatar, S Teraoka, Z Wang, et al.
Blood
|
January 11, 2000
Four novel mutations in the gene encoding gp91-phox of human NADPH oxidase: consequences for oxidase assembly
J H Leusen, C Meischl, M H Eppink, et al.
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of 3