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Genomics
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November 5, 1997
Genomic sequence and organization of the human gene for cytochrome c oxidase subunit (COX7A1) VIIa-M
W Wolz, W Kress, C R Mueller
European Journal of Biochemistry
|
March 1, 1995
Murine liver homogentisate 1,2-dioxygenase. Purification to homogeneity and novel biochemical properties
S R Schmidt, C R Müller, W Kress
Cytogenetics and Cell Genetics
|
August 18, 1999
The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28:report of the first familial case
O Bartsch, W Kress, A Wagner, et al.
Clinical Genetics
|
September 14, 2007
Endocardial cushion defect in a patient with Crouzon syndrome carrying a mutation in the fibroblast growth factor receptor (FGFR)-2 gene
C Schulz, W Kress, A Schömig, et al.
Cytogenetics and Cell Genetics
|
February 15, 2001
An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly
W Kress, B Petersen, H Collmann, et al.
Pediatric Dermatology
|
September 16, 2008
Erythematous crusted plaques in a pediatric transplant recipient
Holly R Mason, Jonhan Ho, Douglas W Kress
Journal of Neurology
|
July 28, 2007
Orthostatic tremor in three brothers
M Fischer, W Kress, K Reiners, et al.
Environmental Monitoring and Assessment
|
November 23, 2013
Growth impact of O3, NO 2 and/or SO 2 on pinus taeda
L W Kress, J M Skelly, K H Hinkelmann
Journal of Neurology
|
March 27, 2001
Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals
G Kuhlenbäumer, W Kress, E B Ringelstein, et al.
Pennsylvania Medicine
|
March 1, 1982
Lower-extremity reconstructive procedures
D W Kress, T S Davis, W P Graham
Page
of 12
Search research articles
Search
Showing results (11-20 of 119) with videos related to
Sort By:
Page
of 12
Genomics
|
November 5, 1997
Genomic sequence and organization of the human gene for cytochrome c oxidase subunit (COX7A1) VIIa-M
W Wolz, W Kress, C R Mueller
European Journal of Biochemistry
|
March 1, 1995
Murine liver homogentisate 1,2-dioxygenase. Purification to homogeneity and novel biochemical properties
S R Schmidt, C R Müller, W Kress
Cytogenetics and Cell Genetics
|
August 18, 1999
The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28:report of the first familial case
O Bartsch, W Kress, A Wagner, et al.
Clinical Genetics
|
September 14, 2007
Endocardial cushion defect in a patient with Crouzon syndrome carrying a mutation in the fibroblast growth factor receptor (FGFR)-2 gene
C Schulz, W Kress, A Schömig, et al.
Cytogenetics and Cell Genetics
|
February 15, 2001
An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly
W Kress, B Petersen, H Collmann, et al.
Pediatric Dermatology
|
September 16, 2008
Erythematous crusted plaques in a pediatric transplant recipient
Holly R Mason, Jonhan Ho, Douglas W Kress
Journal of Neurology
|
July 28, 2007
Orthostatic tremor in three brothers
M Fischer, W Kress, K Reiners, et al.
Environmental Monitoring and Assessment
|
November 23, 2013
Growth impact of O3, NO 2 and/or SO 2 on pinus taeda
L W Kress, J M Skelly, K H Hinkelmann
Journal of Neurology
|
March 27, 2001
Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals
G Kuhlenbäumer, W Kress, E B Ringelstein, et al.
Pennsylvania Medicine
|
March 1, 1982
Lower-extremity reconstructive procedures
D W Kress, T S Davis, W P Graham
Page
of 12