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Oral Diseases
|
November 8, 2023
The value of regular follow-up of oral leukoplakia for early detection of malignant transformation
Ilkay Evren, Ahmad M Najim, Jos B Poell, et al.
Acta Neurologica Belgica
|
February 3, 2010
Organisation of inhospital acute stroke care and minimum criteria for stroke care units. Recommendations of the Belgian Stroke Council
, V Thijs, A Peeters, et al.
Experimental Dermatology
|
March 24, 2018
A rare missense mutation in GJB3 (Cx31G45E) is associated with a unique cellular phenotype resulting in necrotic cell death
Jennifer A Easton, Ahmad K Albuloushi, Miriam A F Kamps, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
January 29, 2005
Toward positional cloning of the curly tail gene
Madeleine R Brouns, Marian C E Peeters, Jan M Geurts, et al.
Cells
|
April 26, 2024
Genomic Engineering of Oral Keratinocytes to Establish In Vitro Oral Potentially Malignant Disease Models as a Platform for Treatment Investigation
Leon J Wils, Marijke Buijze, Marijke Stigter-van Walsum, et al.
Human Molecular Genetics
|
January 26, 2011
Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouse
Madeleine R Brouns, Sandra C P De Castro, Els A Terwindt-Rouwenhorst, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 46) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 46 results.
Oral Diseases
|
November 8, 2023
The value of regular follow-up of oral leukoplakia for early detection of malignant transformation
Ilkay Evren, Ahmad M Najim, Jos B Poell, et al.
Acta Neurologica Belgica
|
February 3, 2010
Organisation of inhospital acute stroke care and minimum criteria for stroke care units. Recommendations of the Belgian Stroke Council
, V Thijs, A Peeters, et al.
Experimental Dermatology
|
March 24, 2018
A rare missense mutation in GJB3 (Cx31G45E) is associated with a unique cellular phenotype resulting in necrotic cell death
Jennifer A Easton, Ahmad K Albuloushi, Miriam A F Kamps, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
January 29, 2005
Toward positional cloning of the curly tail gene
Madeleine R Brouns, Marian C E Peeters, Jan M Geurts, et al.
Cells
|
April 26, 2024
Genomic Engineering of Oral Keratinocytes to Establish In Vitro Oral Potentially Malignant Disease Models as a Platform for Treatment Investigation
Leon J Wils, Marijke Buijze, Marijke Stigter-van Walsum, et al.
Human Molecular Genetics
|
January 26, 2011
Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouse
Madeleine R Brouns, Sandra C P De Castro, Els A Terwindt-Rouwenhorst, et al.
Page
of 5