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D Macaya

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

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Biomedical Materials (Bristol, England)|January 14, 2012
Injectable hydrogel materials for spinal cord regeneration: a reviewD Macaya, M Spector
Heredity|July 18, 2013
Admixture mapping of quantitative traits in Populus hybrid zones: power and limitationsD Lindtke, S C González-Martínez, D Macaya-Sanz, et al.
American Journal of Medical Genetics. Part A|July 3, 2009
A synonymous mutation in TCOF1 causes Treacher Collins syndrome due to mis-splicing of a constitutive exonD Macaya, S H Katsanis, T W Hefferon, et al.
Heredity|May 19, 2011
Genetic analysis of post-mating reproductive barriers in hybridizing European Populus speciesD Macaya-Sanz, L Suter, J Joseph, et al.
Molecular Ecology|May 26, 2012
The Atlantic-Mediterranean watershed, river basins and glacial history shape the genetic structure of Iberian poplarsD Macaya-Sanz, M Heuertz, U López-de-Heredia, et al.
Science Translational Medicine|April 9, 2010
Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndromeB L Loeys, E E Gerber, D Riegert-Johnson, et al.
Pageof 1

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

Sort By:
Pageof 1
Biomedical Materials (Bristol, England)|January 14, 2012
Injectable hydrogel materials for spinal cord regeneration: a reviewD Macaya, M Spector
Heredity|July 18, 2013
Admixture mapping of quantitative traits in Populus hybrid zones: power and limitationsD Lindtke, S C González-Martínez, D Macaya-Sanz, et al.
American Journal of Medical Genetics. Part A|July 3, 2009
A synonymous mutation in TCOF1 causes Treacher Collins syndrome due to mis-splicing of a constitutive exonD Macaya, S H Katsanis, T W Hefferon, et al.
Heredity|May 19, 2011
Genetic analysis of post-mating reproductive barriers in hybridizing European Populus speciesD Macaya-Sanz, L Suter, J Joseph, et al.
Molecular Ecology|May 26, 2012
The Atlantic-Mediterranean watershed, river basins and glacial history shape the genetic structure of Iberian poplarsD Macaya-Sanz, M Heuertz, U López-de-Heredia, et al.
Science Translational Medicine|April 9, 2010
Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndromeB L Loeys, E E Gerber, D Riegert-Johnson, et al.
Pageof 1