C J Tack|P Smits - JoVE Visualize

Showing results (311-320 of 347) with videos related to

Pageof 35

Sort By:

American Journal of Medical Genetics|July 9, 1999

Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysisB C Hamel, A P Smits, B van den Helm, et al.

Cardiovascular Research|November 14, 2003

Conduction slowing by the gap junctional uncoupler carbenoxoloneJoris R de Groot, Thijs Veenstra, Arie O Verkerk, et al.

Journal of Medical Genetics|February 1, 1993

The fragile X syndrome: no evidence for any recent mutationsA P Smits, J C Dreesen, J G Post, et al.

American Journal of Human Genetics|May 1, 1996

Mental status of females with an FMR1 gene full mutationB B de Vries, A M Wiegers, A P Smits, et al.

Journal of Molecular and Cellular Cardiology|May 25, 2005

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two familiesJeroen P P Smits, Tamara T Koopmann, Ronald Wilders, et al.

Nature Nanotechnology|October 8, 2009

Monolayer coverage and channel length set the mobility in self-assembled monolayer field-effect transistorsSimon G J Mathijssen, Edsger C P Smits, Paul A van Hal, et al.

Nano Letters|May 11, 2010

Ordered semiconducting self-assembled monolayers on polymeric surfaces utilized in organic integrated circuitsFatemeh Gholamrezaie, Simon G J Mathijssen, Edsger C P Smits, et al.

Placenta|May 12, 2004

Placental folate transport and binding are not impaired in pregnancies complicated by fetal growth restrictionT M Bisseling, E A P Steegers, J J M van den Heuvel, et al.

American Journal of Medical Genetics|July 9, 1999

X-linked mental retardation: evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric regionH G Yntema, B van den Helm, N V Knoers, et al.

American Heart Journal|May 13, 2015

The effect of an apolipoprotein A-I-containing high-density lipoprotein-mimetic particle (CER-001) on carotid artery wall thickness in patients with homozygous familial hypercholesterolemia: The Modifying Orphan Disease Evaluation (MODE) studyG Kees Hovingh, Loek P Smits, Claudia Stefanutti, et al.

Pageof 35

Showing results (311-320 of 347) with videos related to

Sort By:

Pageof 35

American Journal of Medical Genetics|July 9, 1999

Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysisB C Hamel, A P Smits, B van den Helm, et al.

Cardiovascular Research|November 14, 2003

Conduction slowing by the gap junctional uncoupler carbenoxoloneJoris R de Groot, Thijs Veenstra, Arie O Verkerk, et al.

Journal of Medical Genetics|February 1, 1993

The fragile X syndrome: no evidence for any recent mutationsA P Smits, J C Dreesen, J G Post, et al.

American Journal of Human Genetics|May 1, 1996

Mental status of females with an FMR1 gene full mutationB B de Vries, A M Wiegers, A P Smits, et al.

Journal of Molecular and Cellular Cardiology|May 25, 2005

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two familiesJeroen P P Smits, Tamara T Koopmann, Ronald Wilders, et al.

Nature Nanotechnology|October 8, 2009

Monolayer coverage and channel length set the mobility in self-assembled monolayer field-effect transistorsSimon G J Mathijssen, Edsger C P Smits, Paul A van Hal, et al.

Nano Letters|May 11, 2010

Ordered semiconducting self-assembled monolayers on polymeric surfaces utilized in organic integrated circuitsFatemeh Gholamrezaie, Simon G J Mathijssen, Edsger C P Smits, et al.

Placenta|May 12, 2004

Placental folate transport and binding are not impaired in pregnancies complicated by fetal growth restrictionT M Bisseling, E A P Steegers, J J M van den Heuvel, et al.

American Journal of Medical Genetics|July 9, 1999

X-linked mental retardation: evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric regionH G Yntema, B van den Helm, N V Knoers, et al.

American Heart Journal|May 13, 2015

The effect of an apolipoprotein A-I-containing high-density lipoprotein-mimetic particle (CER-001) on carotid artery wall thickness in patients with homozygous familial hypercholesterolemia: The Modifying Orphan Disease Evaluation (MODE) studyG Kees Hovingh, Loek P Smits, Claudia Stefanutti, et al.

Pageof 35