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D J Halley

Showing results (1-10 of 96) with videos related to

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Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Tuberous sclerosis: between genetic and physical analysisD J Halley
Pediatric Research|November 1, 1995
Complex behavior of simple repeats: the fragile X syndromeB A Oostra, D J Halley
Prenatal Diagnosis|August 1, 1990
Risk calculation of missed prenatal diagnosis of fragile-X syndromeB A Oostra, L A Sandkuyl, D J Halley
American Journal of Human Genetics|July 1, 1980
Correction of I-cell defect by hybridization with lysosomal enzyme deficient human fibroblastsA d'Azzo, D J Halley, A Hoogeveen, et al.
Human Genetics|January 1, 1984
Regional mapping of the human gene for lysosomal alpha-glucosidase by in situ hybridizationD J Halley, A Konings, P Hupkes, et al.
Human Genetics|May 1, 1988
Cystic fibrosis: screening for a DNA deletion by field inversion gel electrophoresisJ Morreau, M Sinaasappel, B A Oostra, et al.
American Journal of Medical Genetics|July 15, 1994
Conservation of CGG region in FMR1 gene in mammalsW Deelen, C Bakker, D J Halley, et al.
Journal of Medical Genetics|December 1, 1992
Computer simulation of linkage and heterogeneity in tuberous sclerosis: a critical evaluation of the collaborative family dataL A Janssen, L A Sandkuijl, J R Sampson, et al.
Experimental Cell Research|October 1, 1980
Intercellular exchange of lysosomal hydrolases between mutant human fibroblasts and other cell typesD J Halley, N Sacchi, A d'Azzo, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 26, 2001
[From gene to disease; TSC1 and TSC2 genes and tuberous sclerosis complex]S Verhoef, D Lindhout, D J Halley, et al.
Pageof 10

Showing results (1-10 of 96) with videos related to

Sort By:
Pageof 10
Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Tuberous sclerosis: between genetic and physical analysisD J Halley
Pediatric Research|November 1, 1995
Complex behavior of simple repeats: the fragile X syndromeB A Oostra, D J Halley
Prenatal Diagnosis|August 1, 1990
Risk calculation of missed prenatal diagnosis of fragile-X syndromeB A Oostra, L A Sandkuyl, D J Halley
American Journal of Human Genetics|July 1, 1980
Correction of I-cell defect by hybridization with lysosomal enzyme deficient human fibroblastsA d'Azzo, D J Halley, A Hoogeveen, et al.
Human Genetics|January 1, 1984
Regional mapping of the human gene for lysosomal alpha-glucosidase by in situ hybridizationD J Halley, A Konings, P Hupkes, et al.
Human Genetics|May 1, 1988
Cystic fibrosis: screening for a DNA deletion by field inversion gel electrophoresisJ Morreau, M Sinaasappel, B A Oostra, et al.
American Journal of Medical Genetics|July 15, 1994
Conservation of CGG region in FMR1 gene in mammalsW Deelen, C Bakker, D J Halley, et al.
Journal of Medical Genetics|December 1, 1992
Computer simulation of linkage and heterogeneity in tuberous sclerosis: a critical evaluation of the collaborative family dataL A Janssen, L A Sandkuijl, J R Sampson, et al.
Experimental Cell Research|October 1, 1980
Intercellular exchange of lysosomal hydrolases between mutant human fibroblasts and other cell typesD J Halley, N Sacchi, A d'Azzo, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 26, 2001
[From gene to disease; TSC1 and TSC2 genes and tuberous sclerosis complex]S Verhoef, D Lindhout, D J Halley, et al.
Pageof 10