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P J Willems

Showing results (21-30 of 183) with videos related to

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Immunology|May 1, 1975
Antibody formation in the mouse induced by hapten-carrier complexesH Snippe, W G Graven, P J Willems
Clinical Genetics|May 11, 2007
Mitochondrial deafnessH Kokotas, M B Petersen, P J Willems
American Journal of Human Genetics|April 1, 1997
Nonsyndromic hearing impairment: unparalleled heterogeneityG Van Camp, P J Willems, R J Smith
Biochemical Genetics|June 1, 1989
Abnormal expression of alpha-L-fucosidase in lymphoid cell lines of fucosidosis patientsR A DiCioccio, J K Darby, P J Willems
Results and Problems in Cell Differentiation|July 22, 1998
The fragile X syndrome and other fragile site disordersR F Kooy, B A Oostra, P J Willems
Human Molecular Genetics|August 1, 1993
Six additional mutations in fucosidosis: three nonsense mutations and three frameshift mutationsH C Seo, P J Willems, J S O'Brien
American Journal of Medical Genetics|August 1, 1987
X-linked hydrocephalusP J Willems, O F Brouwer, I Dijkstra, et al.
Human Molecular Genetics|January 1, 1997
L1-associated diseases: clinical geneticists divide, molecular geneticists uniteE Fransen, G Van Camp, L Vits, et al.
European Journal of Pediatrics|January 1, 1990
The natural history of liver glycogenosis due to phosphorylase kinase deficiency: a longitudinal study of 41 patientsP J Willems, W J Gerver, R Berger, et al.
Immunology|May 1, 1975
Delayed hypersensitivity in the mouse induced by hapten-carrier complexesH Snippe, P J Willems, W G Graven, et al.
Pageof 19

Showing results (21-30 of 183) with videos related to

Sort By:
Pageof 19
Immunology|May 1, 1975
Antibody formation in the mouse induced by hapten-carrier complexesH Snippe, W G Graven, P J Willems
Clinical Genetics|May 11, 2007
Mitochondrial deafnessH Kokotas, M B Petersen, P J Willems
American Journal of Human Genetics|April 1, 1997
Nonsyndromic hearing impairment: unparalleled heterogeneityG Van Camp, P J Willems, R J Smith
Biochemical Genetics|June 1, 1989
Abnormal expression of alpha-L-fucosidase in lymphoid cell lines of fucosidosis patientsR A DiCioccio, J K Darby, P J Willems
Results and Problems in Cell Differentiation|July 22, 1998
The fragile X syndrome and other fragile site disordersR F Kooy, B A Oostra, P J Willems
Human Molecular Genetics|August 1, 1993
Six additional mutations in fucosidosis: three nonsense mutations and three frameshift mutationsH C Seo, P J Willems, J S O'Brien
American Journal of Medical Genetics|August 1, 1987
X-linked hydrocephalusP J Willems, O F Brouwer, I Dijkstra, et al.
Human Molecular Genetics|January 1, 1997
L1-associated diseases: clinical geneticists divide, molecular geneticists uniteE Fransen, G Van Camp, L Vits, et al.
European Journal of Pediatrics|January 1, 1990
The natural history of liver glycogenosis due to phosphorylase kinase deficiency: a longitudinal study of 41 patientsP J Willems, W J Gerver, R Berger, et al.
Immunology|May 1, 1975
Delayed hypersensitivity in the mouse induced by hapten-carrier complexesH Snippe, P J Willems, W G Graven, et al.
Pageof 19