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F Kok

Showing results (21-30 of 106) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|September 28, 2005
[Heterozygosity for alpha1-antitrypsin deficiency as a cofactor in the development of chronic liver disease]K F Kok, P J Wahab, R A de Vries
The Netherlands Journal of Medicine|September 24, 2008
Value of molecular analysis of Wilson's disease in the absence of tissue copper deposits: a novel ATP7B mutation in an adult patientK F Kok, B Hoevenaars, E Waanders, et al.
Genetic Testing|February 24, 2001
Prader-Willi syndrome: genetic tests and clinical findingsC Fridman, M C Varela, F Kok, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 1, 2021
[Ingested medication blister packs]J F de Leijer, D R Geel, K F Kok, et al.
American Journal of Medical Genetics|June 22, 2000
Paternal UPD15: further genetic and clinical studies in four Angelman syndrome patientsC Fridman, M C Varela, F Kok, et al.
Arquivos De Neuro-Psiquiatria|December 1, 1988
[The battered child syndrome: neurologic aspects in 7 cases]C S Miziara, V A Serrano, F Kok, et al.
Physical Review Letters|December 10, 2013
Flux saturation length of sediment transportThomas Pähtz, Jasper F Kok, Eric J R Parteli, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|October 30, 2014
Analytical model for flux saturation in sediment transportThomas Pähtz, Eric J R Parteli, Jasper F Kok, et al.
Nature Communications|January 18, 2018
Global and regional importance of the direct dust-climate feedbackJasper F Kok, Daniel S Ward, Natalie M Mahowald, et al.
Clinical Genetics|December 25, 2004
Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patientsM C Varela, F Kok, N Setian, et al.
Pageof 11

Showing results (21-30 of 106) with videos related to

Sort By:
Pageof 11
Nederlands Tijdschrift Voor Geneeskunde|September 28, 2005
[Heterozygosity for alpha1-antitrypsin deficiency as a cofactor in the development of chronic liver disease]K F Kok, P J Wahab, R A de Vries
The Netherlands Journal of Medicine|September 24, 2008
Value of molecular analysis of Wilson's disease in the absence of tissue copper deposits: a novel ATP7B mutation in an adult patientK F Kok, B Hoevenaars, E Waanders, et al.
Genetic Testing|February 24, 2001
Prader-Willi syndrome: genetic tests and clinical findingsC Fridman, M C Varela, F Kok, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 1, 2021
[Ingested medication blister packs]J F de Leijer, D R Geel, K F Kok, et al.
American Journal of Medical Genetics|June 22, 2000
Paternal UPD15: further genetic and clinical studies in four Angelman syndrome patientsC Fridman, M C Varela, F Kok, et al.
Arquivos De Neuro-Psiquiatria|December 1, 1988
[The battered child syndrome: neurologic aspects in 7 cases]C S Miziara, V A Serrano, F Kok, et al.
Physical Review Letters|December 10, 2013
Flux saturation length of sediment transportThomas Pähtz, Jasper F Kok, Eric J R Parteli, et al.
Physical Review. E, Statistical, Nonlinear, and Soft Matter Physics|October 30, 2014
Analytical model for flux saturation in sediment transportThomas Pähtz, Eric J R Parteli, Jasper F Kok, et al.
Nature Communications|January 18, 2018
Global and regional importance of the direct dust-climate feedbackJasper F Kok, Daniel S Ward, Natalie M Mahowald, et al.
Clinical Genetics|December 25, 2004
Impact of molecular mechanisms, including deletion size, on Prader-Willi syndrome phenotype: study of 75 patientsM C Varela, F Kok, N Setian, et al.
Pageof 11