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The Journal of Surgical Research
|
October 6, 1998
Nitric oxide causes apoptosis in pulmonary vascular smooth muscle cells
J D Smith, S D McLean, D K Nakayama
Biochemistry
|
September 16, 1998
Liposome-cell interactions in vitro: effect of liposome surface charge on the binding and endocytosis of conventional and sterically stabilized liposomes
C R Miller, B Bondurant, S D McLean, et al.
The Pediatric Infectious Disease Journal
|
April 1, 1990
Primary neonatal herpes simplex virus pneumonia
J A Barker, S D McLean, G D Jordan, et al.
American Journal of Diseases of Children (1960)
|
November 1, 1993
Velo-cardio-facial syndrome. Intrafamilial variability of the phenotype
S D McLean, H M Saal, N B Spinner, et al.
Pediatrics
|
January 1, 1996
Learning-disabled males with a fragile X CGG expansion in the upper premutation size range
R J Hagerman, L W Staley, R O'Conner, et al.
Journal of Medical Genetics
|
April 7, 2009
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function
F Lacbawan, B D Solomon, E Roessler, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
The Journal of Surgical Research
|
October 6, 1998
Nitric oxide causes apoptosis in pulmonary vascular smooth muscle cells
J D Smith, S D McLean, D K Nakayama
Biochemistry
|
September 16, 1998
Liposome-cell interactions in vitro: effect of liposome surface charge on the binding and endocytosis of conventional and sterically stabilized liposomes
C R Miller, B Bondurant, S D McLean, et al.
The Pediatric Infectious Disease Journal
|
April 1, 1990
Primary neonatal herpes simplex virus pneumonia
J A Barker, S D McLean, G D Jordan, et al.
American Journal of Diseases of Children (1960)
|
November 1, 1993
Velo-cardio-facial syndrome. Intrafamilial variability of the phenotype
S D McLean, H M Saal, N B Spinner, et al.
Pediatrics
|
January 1, 1996
Learning-disabled males with a fragile X CGG expansion in the upper premutation size range
R J Hagerman, L W Staley, R O'Conner, et al.
Journal of Medical Genetics
|
April 7, 2009
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function
F Lacbawan, B D Solomon, E Roessler, et al.
Page
of 1