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D J Halley

Showing results (41-50 of 96) with videos related to

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Journal of Medical Genetics|December 10, 1997
DNA testing for fragile X syndrome: implications for parents and familyM A van Rijn, B B de Vries, A Tibben, et al.
American Journal of Medical Genetics|September 1, 1991
DNA analysis in patients with lissencephaly type I and other cortical dysplasiasB A Oostra, J F de Rijk-van Andel, H J Eussen, et al.
Human Genetics|December 18, 1998
Screening with the FMR1 protein test among mentally retarded malesB B de Vries, S Mohkamsing, A M van den Ouweland, et al.
Human Reproduction (Oxford, England)|April 1, 1999
The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic dataG R Dohle, H J Veeze, S E Overbeek, et al.
Human Genetics|August 1, 1991
Isolated lissencephaly sequence associated with a microdeletion at chromosome 17p13J F De Rijk-van Andel, C E Catsman-Berrevoets, D J Halley, et al.
Neurology|October 13, 2004
Differential localization of hamartin and tuberin and increased S6 phosphorylation in a tuberF E Jansen, R G E Notenboom, M Nellist, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
Analysis of TSC2 stop codon variants found in tuberous sclerosis patientsM A Goedbloed, M Nellist, B Verhaaf, et al.
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.
Human Genetics|October 1, 1993
Founder effect in a Belgian-Dutch fragile X populationS Buyle, E Reyniers, L Vits, et al.
Pageof 10

Showing results (41-50 of 96) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|December 10, 1997
DNA testing for fragile X syndrome: implications for parents and familyM A van Rijn, B B de Vries, A Tibben, et al.
American Journal of Medical Genetics|September 1, 1991
DNA analysis in patients with lissencephaly type I and other cortical dysplasiasB A Oostra, J F de Rijk-van Andel, H J Eussen, et al.
Human Genetics|December 18, 1998
Screening with the FMR1 protein test among mentally retarded malesB B de Vries, S Mohkamsing, A M van den Ouweland, et al.
Human Reproduction (Oxford, England)|April 1, 1999
The complex relationships between cystic fibrosis and congenital bilateral absence of the vas deferens: clinical, electrophysiological and genetic dataG R Dohle, H J Veeze, S E Overbeek, et al.
Human Genetics|August 1, 1991
Isolated lissencephaly sequence associated with a microdeletion at chromosome 17p13J F De Rijk-van Andel, C E Catsman-Berrevoets, D J Halley, et al.
Neurology|October 13, 2004
Differential localization of hamartin and tuberin and increased S6 phosphorylation in a tuberF E Jansen, R G E Notenboom, M Nellist, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
Analysis of TSC2 stop codon variants found in tuberous sclerosis patientsM A Goedbloed, M Nellist, B Verhaaf, et al.
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.
Human Genetics|October 1, 1993
Founder effect in a Belgian-Dutch fragile X populationS Buyle, E Reyniers, L Vits, et al.
Pageof 10