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The Analyst
|
December 18, 2010
Quantitative SERS sensors for environmental analysis of naphthalene
O Péron, E Rinnert, T Toury, et al.
Journal De Chirurgie
|
January 1, 1996
[Axillary lymphoceles after breast cancer surgery. Pathogeny, prevention]
P Rauch, A L De la Chapelle, A Meunier, et al.
Human Mutation
|
February 5, 2000
The minisatellite expansion mutation in EPM1: resolution of an initial discrepancy. Mutatations in brief no. 186. Online
K Virtaneva, L Paulin, R Krahe, et al.
Genome Research
|
April 1, 1996
Dominantly and recessively inherited cornea plana congenita map to the same small region of chromosome 12
E Tahvanainen, A S Villanueva, H Forsius, et al.
Clinical Genetics
|
October 1, 1985
Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis
A de la Chapelle, E M Sankila, M Lindlöf, et al.
American Journal of Human Genetics
|
May 1, 1985
Segregation and fertility analysis in an autosomal reciprocal translocation, t(1;8)(q41;q23.1)
A E Vauhkonen, E M Sankila, K O Simola, et al.
Pediatrie
|
January 1, 1988
[Stickler's syndrome or hereditary progressive arthro-ophthalmopathy]
A C De la Chapelle, S Manouvrier, J P Dubos, et al.
Analytical Chemistry
|
October 19, 2018
THz Spectroscopy for a Rapid and Label-Free Cell Viability Assay in a Microfluidic Chip Based on an Optical Clearing Agent
Ke Yang, Xiang Yang, Xiang Zhao, et al.
Optics Express
|
October 6, 2012
Optimized plasmonic nanostructures for improved sensing activities
Hong Shen, Nicolas Guillot, Jérémy Rouxel, et al.
Journal of Medical Genetics
|
December 1, 1995
Phenylketonuria in a low incidence population: molecular characterisation of mutations in Finland
P Guldberg, K F Henriksen, I Sipilä, et al.
Page
of 61
Search research articles
Search
Showing results (121-130 of 603) with videos related to
Sort By:
Page
of 61
The Analyst
|
December 18, 2010
Quantitative SERS sensors for environmental analysis of naphthalene
O Péron, E Rinnert, T Toury, et al.
Journal De Chirurgie
|
January 1, 1996
[Axillary lymphoceles after breast cancer surgery. Pathogeny, prevention]
P Rauch, A L De la Chapelle, A Meunier, et al.
Human Mutation
|
February 5, 2000
The minisatellite expansion mutation in EPM1: resolution of an initial discrepancy. Mutatations in brief no. 186. Online
K Virtaneva, L Paulin, R Krahe, et al.
Genome Research
|
April 1, 1996
Dominantly and recessively inherited cornea plana congenita map to the same small region of chromosome 12
E Tahvanainen, A S Villanueva, H Forsius, et al.
Clinical Genetics
|
October 1, 1985
Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis
A de la Chapelle, E M Sankila, M Lindlöf, et al.
American Journal of Human Genetics
|
May 1, 1985
Segregation and fertility analysis in an autosomal reciprocal translocation, t(1;8)(q41;q23.1)
A E Vauhkonen, E M Sankila, K O Simola, et al.
Pediatrie
|
January 1, 1988
[Stickler's syndrome or hereditary progressive arthro-ophthalmopathy]
A C De la Chapelle, S Manouvrier, J P Dubos, et al.
Analytical Chemistry
|
October 19, 2018
THz Spectroscopy for a Rapid and Label-Free Cell Viability Assay in a Microfluidic Chip Based on an Optical Clearing Agent
Ke Yang, Xiang Yang, Xiang Zhao, et al.
Optics Express
|
October 6, 2012
Optimized plasmonic nanostructures for improved sensing activities
Hong Shen, Nicolas Guillot, Jérémy Rouxel, et al.
Journal of Medical Genetics
|
December 1, 1995
Phenylketonuria in a low incidence population: molecular characterisation of mutations in Finland
P Guldberg, K F Henriksen, I Sipilä, et al.
Page
of 61