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Nucleic Acids Research
|
November 11, 1986
DraI RFLP in the human apolipoprotein AI-CIII-AIV gene complex
P M Frossard, R T Coleman, N A Dillan, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
July 1, 1994
Sex-specific effects of the glutamine/histidine polymorphism in apo A-IV on HDL metabolism
A von Eckardstein, H Funke, A Chirazi, et al.
Atherosclerosis
|
February 1, 1991
Molecular basis of lipoprotein lipase deficiency in two Austrian families with type I hyperlipoproteinemia
B Paulweber, H Wiebusch, G Miesenboeck, et al.
Human Mutation
|
January 1, 1994
Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestries
Y Ma, M S Liu, D Chitayat, et al.
Pacing and Clinical Electrophysiology : PACE
|
May 9, 2001
Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndrome
G Moennig, E Schulze-Bahr, H Wedekind, et al.
Journal of Pharmaceutical Sciences
|
January 26, 2022
Atomic-Layer Deposition Processes Applied to Phage λ and a Phage-like Particle Platform Yield Thermostable, Single-Shot Vaccines
Alyssa E Witeof, Wynton D McClary, Laura T Rea, et al.
Clinical Chemistry
|
February 11, 2016
Classifying Germline Sequence Variants in the Era of Next-Generation Sequencing
Linnea M Baudhuin, Birgit H Funke, Lora H Bean, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
July 17, 2012
Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrations
Sa Muntoni, H Wiebusch, M Jansen-Rust, et al.
The Journal of Molecular Diagnostics : JMD
|
December 16, 2023
Slice Testing-Considerations from Ordering to Reporting: A Joint Report of the Association for Molecular Pathology, College of American Pathologists, and National Society of Genetic Counselors
Jeffrey A SoRelle, Birgit H Funke, Celeste C Eno, et al.
Zeitschrift Fur Kardiologie
|
July 23, 2002
[Clinical aspects and molecular genetics of the Jervell- and Lange-Nielsen Syndrome]
G Mönnig, E Schulze-Bahr, H Wedekind, et al.
Page
of 21
Search research articles
Search
Showing results (141-150 of 203) with videos related to
Sort By:
Page
of 21
Nucleic Acids Research
|
November 11, 1986
DraI RFLP in the human apolipoprotein AI-CIII-AIV gene complex
P M Frossard, R T Coleman, N A Dillan, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
July 1, 1994
Sex-specific effects of the glutamine/histidine polymorphism in apo A-IV on HDL metabolism
A von Eckardstein, H Funke, A Chirazi, et al.
Atherosclerosis
|
February 1, 1991
Molecular basis of lipoprotein lipase deficiency in two Austrian families with type I hyperlipoproteinemia
B Paulweber, H Wiebusch, G Miesenboeck, et al.
Human Mutation
|
January 1, 1994
Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestries
Y Ma, M S Liu, D Chitayat, et al.
Pacing and Clinical Electrophysiology : PACE
|
May 9, 2001
Clinical value of electrocardiographic parameters in genotyped individuals with familial long QT syndrome
G Moennig, E Schulze-Bahr, H Wedekind, et al.
Journal of Pharmaceutical Sciences
|
January 26, 2022
Atomic-Layer Deposition Processes Applied to Phage λ and a Phage-like Particle Platform Yield Thermostable, Single-Shot Vaccines
Alyssa E Witeof, Wynton D McClary, Laura T Rea, et al.
Clinical Chemistry
|
February 11, 2016
Classifying Germline Sequence Variants in the Era of Next-Generation Sequencing
Linnea M Baudhuin, Birgit H Funke, Lora H Bean, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
July 17, 2012
Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrations
Sa Muntoni, H Wiebusch, M Jansen-Rust, et al.
The Journal of Molecular Diagnostics : JMD
|
December 16, 2023
Slice Testing-Considerations from Ordering to Reporting: A Joint Report of the Association for Molecular Pathology, College of American Pathologists, and National Society of Genetic Counselors
Jeffrey A SoRelle, Birgit H Funke, Celeste C Eno, et al.
Zeitschrift Fur Kardiologie
|
July 23, 2002
[Clinical aspects and molecular genetics of the Jervell- and Lange-Nielsen Syndrome]
G Mönnig, E Schulze-Bahr, H Wedekind, et al.
Page
of 21