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Journal of Thrombosis and Haemostasis : JTH
|
August 26, 2010
Characterization of duplication breakpoints in the factor VIII gene
M A Zimmermann, J Oldenburg, C R Müller, et al.
The British Journal of Dermatology
|
December 1, 1981
X-linked recessive ichthyosis in three sisters: evidence for homozygosity
B Mevorah, E Frenk, C R Müller, et al.
Human Genetics
|
January 1, 1980
X-linked steroid sulfatase: evidence for different gene-dosage in males and females
C R Müller, B Migl, H Traupe, et al.
Acta Anaesthesiologica Scandinavica
|
November 4, 2006
Malignant hyperthermia and central core disease causative mutations in Swedish patients
M Broman, G Islander, C R Müller, et al.
The British Journal of Dermatology
|
January 17, 2007
Phototoxic reaction and porphyrin fluorescence in skin after topical application of methyl aminolaevulinate
E Angell-Petersen, C Christensen, C R Müller, et al.
Hamostaseologie
|
November 9, 2016
Mutational spectrum and deep intronic variants in the factor VIII gene of haemophilia A patients. Identification by next generation sequencing
J E Bach, J Oldenburg, C R Müller, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
March 8, 2014
Expression studies of mutant factor VIII alleles with premature termination codons with regard to inhibitor formation
M A Zimmermann, J Oldenburg, C R Müller, et al.
Cytogenetics and Cell Genetics
|
January 1, 1983
An XX male with a single STS gene dose
P Wieacker, J Voiculescu, C R Müller, et al.
Human Molecular Genetics
|
August 1, 1992
Dinucleotide repeat polymorphism at the human gene for the brain-derived neurotrophic factor (BDNF)
M Pröschel, A Saunders, A D Roses, et al.
Cytogenetics and Cell Genetics
|
January 1, 1981
Steroid sulfatase activity in cultured fibroblasts of XX males
H H Ropers, B Migl, J Zimmer, et al.
Page
of 15
Search research articles
Search
Showing results (31-40 of 143) with videos related to
Sort By:
Page
of 15
Journal of Thrombosis and Haemostasis : JTH
|
August 26, 2010
Characterization of duplication breakpoints in the factor VIII gene
M A Zimmermann, J Oldenburg, C R Müller, et al.
The British Journal of Dermatology
|
December 1, 1981
X-linked recessive ichthyosis in three sisters: evidence for homozygosity
B Mevorah, E Frenk, C R Müller, et al.
Human Genetics
|
January 1, 1980
X-linked steroid sulfatase: evidence for different gene-dosage in males and females
C R Müller, B Migl, H Traupe, et al.
Acta Anaesthesiologica Scandinavica
|
November 4, 2006
Malignant hyperthermia and central core disease causative mutations in Swedish patients
M Broman, G Islander, C R Müller, et al.
The British Journal of Dermatology
|
January 17, 2007
Phototoxic reaction and porphyrin fluorescence in skin after topical application of methyl aminolaevulinate
E Angell-Petersen, C Christensen, C R Müller, et al.
Hamostaseologie
|
November 9, 2016
Mutational spectrum and deep intronic variants in the factor VIII gene of haemophilia A patients. Identification by next generation sequencing
J E Bach, J Oldenburg, C R Müller, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
March 8, 2014
Expression studies of mutant factor VIII alleles with premature termination codons with regard to inhibitor formation
M A Zimmermann, J Oldenburg, C R Müller, et al.
Cytogenetics and Cell Genetics
|
January 1, 1983
An XX male with a single STS gene dose
P Wieacker, J Voiculescu, C R Müller, et al.
Human Molecular Genetics
|
August 1, 1992
Dinucleotide repeat polymorphism at the human gene for the brain-derived neurotrophic factor (BDNF)
M Pröschel, A Saunders, A D Roses, et al.
Cytogenetics and Cell Genetics
|
January 1, 1981
Steroid sulfatase activity in cultured fibroblasts of XX males
H H Ropers, B Migl, J Zimmer, et al.
Page
of 15