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Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 9, 1991
Specific diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in dried blood spots by a polymerase chain reaction (PCR) assay detecting a point-mutation (G985) in the MCAD gene
N Gregersen, A I Blakemore, V Winter, et al.
The European Respiratory Journal
|
May 1, 1992
Alpha 1-antitrypsin alleles in patients with pulmonary emphysema, detected by DNA amplification (PCR) and oligonucleotide probes
K Bruun-Petersen, G Bruun-Petersen, R Dahl, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 30, 1989
Detection of point mutations in amplified single copy genes by biotin-labelled oligonucleotides: diagnosis of variants of alpha-1-antitrypsin
N Gregersen, V Winter, K B Petersen, et al.
Clinical Genetics
|
April 1, 1996
Two novel mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in a Spanish population
A Cenarro, H K Jensen, F Civeira, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 11, 1981
Urinary excretion of succinylacetone and delta-aminolevulinic acid in patients with hereditary tyrosinemia
E Christensen, B B Jacobsen, N Gregersen, et al.
Human Mutation
|
August 29, 2001
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship
N Gregersen, B S Andresen, M J Corydon, et al.
Archives of Disease in Childhood
|
December 22, 2000
A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiency
E H Touma, M S Rashed, C Vianey-Saban, et al.
Nature Nanotechnology
|
March 25, 2014
Random nanolasing in the Anderson localized regime
J Liu, P D Garcia, S Ek, et al.
Clinical Genetics
|
March 1, 1990
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization
J Koch, S Kølvraa, N Hobolt, et al.
Biochimica Et Biophysica Acta
|
October 13, 1992
Expression of wild-type and mutant medium-chain acyl-CoA dehydrogenase (MCAD) cDNA in eucaryotic cells
T G Jensen, B S Andresen, P Bross, et al.
Page
of 21
Search research articles
Search
Showing results (131-140 of 208) with videos related to
Sort By:
Page
of 21
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 9, 1991
Specific diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in dried blood spots by a polymerase chain reaction (PCR) assay detecting a point-mutation (G985) in the MCAD gene
N Gregersen, A I Blakemore, V Winter, et al.
The European Respiratory Journal
|
May 1, 1992
Alpha 1-antitrypsin alleles in patients with pulmonary emphysema, detected by DNA amplification (PCR) and oligonucleotide probes
K Bruun-Petersen, G Bruun-Petersen, R Dahl, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 30, 1989
Detection of point mutations in amplified single copy genes by biotin-labelled oligonucleotides: diagnosis of variants of alpha-1-antitrypsin
N Gregersen, V Winter, K B Petersen, et al.
Clinical Genetics
|
April 1, 1996
Two novel mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in a Spanish population
A Cenarro, H K Jensen, F Civeira, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 11, 1981
Urinary excretion of succinylacetone and delta-aminolevulinic acid in patients with hereditary tyrosinemia
E Christensen, B B Jacobsen, N Gregersen, et al.
Human Mutation
|
August 29, 2001
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship
N Gregersen, B S Andresen, M J Corydon, et al.
Archives of Disease in Childhood
|
December 22, 2000
A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiency
E H Touma, M S Rashed, C Vianey-Saban, et al.
Nature Nanotechnology
|
March 25, 2014
Random nanolasing in the Anderson localized regime
J Liu, P D Garcia, S Ek, et al.
Clinical Genetics
|
March 1, 1990
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization
J Koch, S Kølvraa, N Hobolt, et al.
Biochimica Et Biophysica Acta
|
October 13, 1992
Expression of wild-type and mutant medium-chain acyl-CoA dehydrogenase (MCAD) cDNA in eucaryotic cells
T G Jensen, B S Andresen, P Bross, et al.
Page
of 21