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American Journal of Human Genetics
|
October 1, 1990
Benign missense variations in the cystic fibrosis gene
K Kobayashi, M R Knowles, R C Boucher, et al.
American Journal of Human Genetics
|
June 1, 1988
Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA
H Y Zoghbi, S P Daiger, A McCall, et al.
The Journal of Biological Chemistry
|
July 5, 1990
Heterogeneity of mutations in argininosuccinate synthetase causing human citrullinemia
K Kobayashi, M J Jackson, D B Tick, et al.
Clinical Chemistry
|
October 31, 2002
Use of denaturing HPLC to provide efficient detection of mutations causing familial hypercholesterolemia
Olaf A Bodamer, Dan Bercovich, Michael Schlabach, et al.
Human Mutation
|
January 1, 1994
A robotics-assisted procedure for large scale cystic fibrosis mutation analysis
J M DeMarchi, C S Richards, R G Fenwick, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
April 30, 2003
Reduced inflammation and improved airway expression using helper-dependent adenoviral vectors with a K18 promoter
Gabriele Toietta, David R Koehler, Milton J Finegold, et al.
The Journal of Pediatrics
|
March 1, 1975
Variation in the phenotypic expression of beta-glucuronidase deficiency
A L Beaudet, N M DiFerrante, G D Ferry, et al.
Human Molecular Genetics
|
September 25, 1997
X-linked glycerol kinase deficiency in the mouse leads to growth retardation, altered fat metabolism, autonomous glucocorticoid secretion and neonatal death
A H Huq, R S Lovell, C N Ou, et al.
The Canadian Journal of Cardiology
|
October 1, 1988
Medtronic-Hall prosthesis: valve related deaths and complications
R L Beaudet, G Nakhle, C R Beaulieu, et al.
Obesity Research
|
July 2, 2004
Leukocyte migration in adipose tissue of mice null for ICAM-1 and Mac-1 adhesion receptors
Rebecca L Robker, Robert G Collins, Arthur L Beaudet, et al.
Page
of 46
Search research articles
Search
Showing results (191-200 of 456) with videos related to
Sort By:
Page
of 46
American Journal of Human Genetics
|
October 1, 1990
Benign missense variations in the cystic fibrosis gene
K Kobayashi, M R Knowles, R C Boucher, et al.
American Journal of Human Genetics
|
June 1, 1988
Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA
H Y Zoghbi, S P Daiger, A McCall, et al.
The Journal of Biological Chemistry
|
July 5, 1990
Heterogeneity of mutations in argininosuccinate synthetase causing human citrullinemia
K Kobayashi, M J Jackson, D B Tick, et al.
Clinical Chemistry
|
October 31, 2002
Use of denaturing HPLC to provide efficient detection of mutations causing familial hypercholesterolemia
Olaf A Bodamer, Dan Bercovich, Michael Schlabach, et al.
Human Mutation
|
January 1, 1994
A robotics-assisted procedure for large scale cystic fibrosis mutation analysis
J M DeMarchi, C S Richards, R G Fenwick, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
April 30, 2003
Reduced inflammation and improved airway expression using helper-dependent adenoviral vectors with a K18 promoter
Gabriele Toietta, David R Koehler, Milton J Finegold, et al.
The Journal of Pediatrics
|
March 1, 1975
Variation in the phenotypic expression of beta-glucuronidase deficiency
A L Beaudet, N M DiFerrante, G D Ferry, et al.
Human Molecular Genetics
|
September 25, 1997
X-linked glycerol kinase deficiency in the mouse leads to growth retardation, altered fat metabolism, autonomous glucocorticoid secretion and neonatal death
A H Huq, R S Lovell, C N Ou, et al.
The Canadian Journal of Cardiology
|
October 1, 1988
Medtronic-Hall prosthesis: valve related deaths and complications
R L Beaudet, G Nakhle, C R Beaulieu, et al.
Obesity Research
|
July 2, 2004
Leukocyte migration in adipose tissue of mice null for ICAM-1 and Mac-1 adhesion receptors
Rebecca L Robker, Robert G Collins, Arthur L Beaudet, et al.
Page
of 46