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D J Halley

Showing results (51-60 of 96) with videos related to

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Human Genetics|March 1, 1996
Angelman syndrome in an inbred familyJ Beuten, R C Hennekam, B Van Roy, 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.
Oncogene|February 15, 2001
The tuberous sclerosis-1 (TSC1) gene product hamartin suppresses cell growth and augments the expression of the TSC2 product tuberin by inhibiting its ubiquitinationG Benvenuto, S Li, S J Brown, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 31, 1997
Common C-to-T substitution at position -480 of the hepatic lipase promoter associated with a lowered lipase activity in coronary artery disease patientsH Jansen, A J Verhoeven, L Weeks, et al.
Genomics|January 1, 1990
New polymorphic DNA marker close to the fragile site FRAXAB A Oostra, P E Hupkes, L F Perdon, et al.
Prenatal Diagnosis|August 26, 1998
Uniparental disomy with and without confined placental mosaicism: a model for trisomic zygote rescueF J Los, D van Opstal, C van den Berg, et al.
Human Genetics|September 1, 1996
Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populationsH G de Vries, M A van der Meulen, R Rozen, et al.
Prenatal Diagnosis|April 21, 1999
Amniocentesis or chorionic villus sampling in multiple gestations? Experience with 500 casesC van den Berg, A P Braat, D Van Opstal, et al.
The Journal of Clinical Investigation|December 26, 2001
Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblingsI Bronsveld, F Mekus, J Bijman, et al.
Pageof 10

Showing results (51-60 of 96) with videos related to

Sort By:
Pageof 10
Human Genetics|March 1, 1996
Angelman syndrome in an inbred familyJ Beuten, R C Hennekam, B Van Roy, 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.
Oncogene|February 15, 2001
The tuberous sclerosis-1 (TSC1) gene product hamartin suppresses cell growth and augments the expression of the TSC2 product tuberin by inhibiting its ubiquitinationG Benvenuto, S Li, S J Brown, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 31, 1997
Common C-to-T substitution at position -480 of the hepatic lipase promoter associated with a lowered lipase activity in coronary artery disease patientsH Jansen, A J Verhoeven, L Weeks, et al.
Genomics|January 1, 1990
New polymorphic DNA marker close to the fragile site FRAXAB A Oostra, P E Hupkes, L F Perdon, et al.
Prenatal Diagnosis|August 26, 1998
Uniparental disomy with and without confined placental mosaicism: a model for trisomic zygote rescueF J Los, D van Opstal, C van den Berg, et al.
Human Genetics|September 1, 1996
Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populationsH G de Vries, M A van der Meulen, R Rozen, et al.
Prenatal Diagnosis|April 21, 1999
Amniocentesis or chorionic villus sampling in multiple gestations? Experience with 500 casesC van den Berg, A P Braat, D Van Opstal, et al.
The Journal of Clinical Investigation|December 26, 2001
Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblingsI Bronsveld, F Mekus, J Bijman, et al.
Pageof 10