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S D McLean

Showing results (1-10 of 6) with videos related to

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The Journal of Surgical Research|October 6, 1998
Nitric oxide causes apoptosis in pulmonary vascular smooth muscle cellsJ 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 liposomesC R Miller, B Bondurant, S D McLean, et al.
The Pediatric Infectious Disease Journal|April 1, 1990
Primary neonatal herpes simplex virus pneumoniaJ 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 phenotypeS 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 rangeR 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 functionF Lacbawan, B D Solomon, E Roessler, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
The Journal of Surgical Research|October 6, 1998
Nitric oxide causes apoptosis in pulmonary vascular smooth muscle cellsJ 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 liposomesC R Miller, B Bondurant, S D McLean, et al.
The Pediatric Infectious Disease Journal|April 1, 1990
Primary neonatal herpes simplex virus pneumoniaJ 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 phenotypeS 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 rangeR 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 functionF Lacbawan, B D Solomon, E Roessler, et al.
Pageof 1