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S J Chin

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

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ISA Transactions|January 28, 2003
Feedforward suppression of force ripple based on a simplex-optimized dither signalK K Tan, S J Chin, H F Dou
Journal of Clinical Psychopharmacology|February 1, 1992
Fluoxetine in social phobiaF R Schneier, S J Chin, E Hollander, et al.
The Journal of Clinical Investigation|December 1, 1988
Hypoxanthine-guanine phosphoribosyltransferase. Genetic evidence for identical mutations in two partially deficient subjectsB L Davidson, S J Chin, J M Wilson, et al.
Prenatal Diagnosis|April 21, 1999
Prenatal diagnosis of mucolipidosis II--electron microscopy and biochemical evaluationW F Carey, A Jaunzems, M Richardson, et al.
Human Genetics|September 10, 1999
A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotypeM A Maxwell, P V Nelson, S J Chin, et al.
Prenatal Diagnosis|December 10, 2003
Analysis of CFTR mutation screening in cases of isolated fetal echogenic bowel in the South Australian populationC M Nicholls, P V Nelson, N K Poplawski, et al.
Pageof 1

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

Sort By:
Pageof 1
ISA Transactions|January 28, 2003
Feedforward suppression of force ripple based on a simplex-optimized dither signalK K Tan, S J Chin, H F Dou
Journal of Clinical Psychopharmacology|February 1, 1992
Fluoxetine in social phobiaF R Schneier, S J Chin, E Hollander, et al.
The Journal of Clinical Investigation|December 1, 1988
Hypoxanthine-guanine phosphoribosyltransferase. Genetic evidence for identical mutations in two partially deficient subjectsB L Davidson, S J Chin, J M Wilson, et al.
Prenatal Diagnosis|April 21, 1999
Prenatal diagnosis of mucolipidosis II--electron microscopy and biochemical evaluationW F Carey, A Jaunzems, M Richardson, et al.
Human Genetics|September 10, 1999
A common PEX1 frameshift mutation in patients with disorders of peroxisome biogenesis correlates with the severe Zellweger syndrome phenotypeM A Maxwell, P V Nelson, S J Chin, et al.
Prenatal Diagnosis|December 10, 2003
Analysis of CFTR mutation screening in cases of isolated fetal echogenic bowel in the South Australian populationC M Nicholls, P V Nelson, N K Poplawski, et al.
Pageof 1