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Annales De L'Institut Pasteur. Immunology
|
September 1, 1988
Polymorphism of the seventh component of complement (C7) in a healthy Caucasian population: an immunoblotting study with neuraminidase-treated samples
G Dewald
Vox Sanguinis
|
January 1, 1979
Polymorphism of the second component of human complement (C2). Observation of the rare phenotype (C2 2 (= C2 B) and data on the localization of the C2 locus in the HLA region
G Dewald, C Rittner
Birth Defects Original Article Series
|
January 1, 1974
Automated videodensitometry of human chromosomes
H Gordon, G Dewald
Human Molecular Genetics
|
January 1, 1994
A common amino acid polymorphism in complement component C1R
M M Nöthen, G Dewald
American Journal of Medical Genetics
|
March 1, 1994
Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomalies
A R Melnyk, G Dewald
Clinical Genetics
|
March 1, 1995
Dinucleotide repeat polymorphism at the human CD59 locus
M M Nöthen, G Dewald
The British Journal of Dermatology
|
February 1, 2006
Hereditary angio-oedema with normal C1 inhibitor in a family with affected women and men
K Bork, D Gül, G Dewald
Archives of Dermatology
|
May 1, 1978
Sister chromatid exchanges in Bloom's syndrome
C H Dicken, G Dewald, H Gordon
Biochemical and Biophysical Research Communications
|
July 15, 1993
Polymorphism of human complement component C6: an amino acid substitution (Glu/Ala) within the second thrombospondin repeat differentiates between the two common allotypes C6 A and C6 B
G Dewald, M M Nöthen, S Cichon
FEBS Letters
|
March 7, 1994
Human complement component C8. Molecular basis of the beta-chain polymorphism
G Dewald, S Hemmer, M M Nöthen
Page
of 6
Search research articles
Search
Showing results (1-10 of 57) with videos related to
Sort By:
Page
of 6
Annales De L'Institut Pasteur. Immunology
|
September 1, 1988
Polymorphism of the seventh component of complement (C7) in a healthy Caucasian population: an immunoblotting study with neuraminidase-treated samples
G Dewald
Vox Sanguinis
|
January 1, 1979
Polymorphism of the second component of human complement (C2). Observation of the rare phenotype (C2 2 (= C2 B) and data on the localization of the C2 locus in the HLA region
G Dewald, C Rittner
Birth Defects Original Article Series
|
January 1, 1974
Automated videodensitometry of human chromosomes
H Gordon, G Dewald
Human Molecular Genetics
|
January 1, 1994
A common amino acid polymorphism in complement component C1R
M M Nöthen, G Dewald
American Journal of Medical Genetics
|
March 1, 1994
Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomalies
A R Melnyk, G Dewald
Clinical Genetics
|
March 1, 1995
Dinucleotide repeat polymorphism at the human CD59 locus
M M Nöthen, G Dewald
The British Journal of Dermatology
|
February 1, 2006
Hereditary angio-oedema with normal C1 inhibitor in a family with affected women and men
K Bork, D Gül, G Dewald
Archives of Dermatology
|
May 1, 1978
Sister chromatid exchanges in Bloom's syndrome
C H Dicken, G Dewald, H Gordon
Biochemical and Biophysical Research Communications
|
July 15, 1993
Polymorphism of human complement component C6: an amino acid substitution (Glu/Ala) within the second thrombospondin repeat differentiates between the two common allotypes C6 A and C6 B
G Dewald, M M Nöthen, S Cichon
FEBS Letters
|
March 7, 1994
Human complement component C8. Molecular basis of the beta-chain polymorphism
G Dewald, S Hemmer, M M Nöthen
Page
of 6