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European Journal of Pediatrics
|
September 8, 2001
Quality control in mutation analysis: the European Molecular Genetics Quality Network (EMQN)
C R Müller,
Zeitschrift Fur Kardiologie
|
January 1, 1994
[Principles, possibilities and limits of gene therapy]
C R Müller-Reible
Klinische Padiatrie
|
January 1, 1994
[Indirect molecular-genetic family study and prenatal diagnosis of infantile spinal muscular atrophy]
U Heber, C R Müller
Nucleic Acids Research
|
August 25, 1989
An MspI polymorphism for the dystrophin intragenic probe J-47
G Meng, C R Müller
Genomics
|
May 1, 1989
Identification of a 220-kb insertion into the Duchenne gene in a family with an atypical course of muscular dystrophy
T Bettecken, C R Müller
Human Genetics
|
October 1, 1986
Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy families
C R Müller, T Grimm
Human Immunology
|
January 1, 1991
How many probes are needed for HLA-DPB1 typing with sequence-specific oligonucleotide probes? A theoretical approach using computer simulation
C R Müller, T H Eiermann
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|
February 2, 2013
Is axial dispersion within rotating cylinders governed by the Froude number?
J R Third, C R Müller
Human Genetics
|
January 1, 1980
Linkage of genes for chronic granulomatous disease and Xg
G Wolff, C R Müller, A Jobke
FEBS Letters
|
July 15, 1974
Rapid isolation of a plant microsomal fraction by Mg2+--precipitation
H Diesperger, C R Müller, H Sandermann
Page
of 15
Search research articles
Search
Showing results (1-10 of 143) with videos related to
Sort By:
Page
of 15
European Journal of Pediatrics
|
September 8, 2001
Quality control in mutation analysis: the European Molecular Genetics Quality Network (EMQN)
C R Müller,
Zeitschrift Fur Kardiologie
|
January 1, 1994
[Principles, possibilities and limits of gene therapy]
C R Müller-Reible
Klinische Padiatrie
|
January 1, 1994
[Indirect molecular-genetic family study and prenatal diagnosis of infantile spinal muscular atrophy]
U Heber, C R Müller
Nucleic Acids Research
|
August 25, 1989
An MspI polymorphism for the dystrophin intragenic probe J-47
G Meng, C R Müller
Genomics
|
May 1, 1989
Identification of a 220-kb insertion into the Duchenne gene in a family with an atypical course of muscular dystrophy
T Bettecken, C R Müller
Human Genetics
|
October 1, 1986
Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy families
C R Müller, T Grimm
Human Immunology
|
January 1, 1991
How many probes are needed for HLA-DPB1 typing with sequence-specific oligonucleotide probes? A theoretical approach using computer simulation
C R Müller, T H Eiermann
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics
|
February 2, 2013
Is axial dispersion within rotating cylinders governed by the Froude number?
J R Third, C R Müller
Human Genetics
|
January 1, 1980
Linkage of genes for chronic granulomatous disease and Xg
G Wolff, C R Müller, A Jobke
FEBS Letters
|
July 15, 1974
Rapid isolation of a plant microsomal fraction by Mg2+--precipitation
H Diesperger, C R Müller, H Sandermann
Page
of 15