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J Halley

Showing results (101-110 of 194) with videos related to

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Epilepsia|August 1, 1997
Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndromeG M Terwindt, R A Ophoff, D Lindhout, et al.
Lancet (London, England)|October 21, 1989
Prenatal detection of major cystic fibrosis mutationD J Halley, N H van Damme, W H Deelen, et al.
Pharmaceutics|May 24, 2017
Optimizing Prednisolone Loading into Distiller's Dried Grain Kafirin Microparticles, and In vitro Release for Oral DeliveryEsther T L Lau, Stuart K Johnson, Barbara A Williams, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|August 24, 2010
Combined cardiological and neurological abnormalities due to filamin A gene mutationMarie Claire Y de Wit, Irenaeus F M de Coo, Maarten H Lequin, et al.
Human Genetics|October 1, 1993
Founder effect in a Belgian-Dutch fragile X populationS Buyle, E Reyniers, L Vits, et al.
Human Genetics|March 1, 1996
Angelman syndrome in an inbred familyJ Beuten, R C Hennekam, B Van Roy, et al.
Journal of Medical Genetics|April 5, 2003
Studies on the pathogenesis of Costello syndromeG M S Mancini, O P van Diggelen, W J Kleijer, et al.
Human Genetics|September 1, 1990
The mutation delta F508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosisD J Halley, H J Veeze, L A Sandkuyl, et al.
Human Molecular Genetics|October 1, 1994
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomesA M van den Ouweland, W H Deelen, C B Kunst, et al.
Clinical Genetics|May 10, 2013
A clinical and genetic overview of 18 years neurofibromatosis type 1 molecular diagnostics in the NetherlandsR van Minkelen, Y van Bever, J N R Kromosoeto, et al.
Pageof 20

Showing results (101-110 of 194) with videos related to

Sort By:
Pageof 20
Epilepsia|August 1, 1997
Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndromeG M Terwindt, R A Ophoff, D Lindhout, et al.
Lancet (London, England)|October 21, 1989
Prenatal detection of major cystic fibrosis mutationD J Halley, N H van Damme, W H Deelen, et al.
Pharmaceutics|May 24, 2017
Optimizing Prednisolone Loading into Distiller's Dried Grain Kafirin Microparticles, and In vitro Release for Oral DeliveryEsther T L Lau, Stuart K Johnson, Barbara A Williams, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|August 24, 2010
Combined cardiological and neurological abnormalities due to filamin A gene mutationMarie Claire Y de Wit, Irenaeus F M de Coo, Maarten H Lequin, et al.
Human Genetics|October 1, 1993
Founder effect in a Belgian-Dutch fragile X populationS Buyle, E Reyniers, L Vits, et al.
Human Genetics|March 1, 1996
Angelman syndrome in an inbred familyJ Beuten, R C Hennekam, B Van Roy, et al.
Journal of Medical Genetics|April 5, 2003
Studies on the pathogenesis of Costello syndromeG M S Mancini, O P van Diggelen, W J Kleijer, et al.
Human Genetics|September 1, 1990
The mutation delta F508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosisD J Halley, H J Veeze, L A Sandkuyl, et al.
Human Molecular Genetics|October 1, 1994
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomesA M van den Ouweland, W H Deelen, C B Kunst, et al.
Clinical Genetics|May 10, 2013
A clinical and genetic overview of 18 years neurofibromatosis type 1 molecular diagnostics in the NetherlandsR van Minkelen, Y van Bever, J N R Kromosoeto, et al.
Pageof 20