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P L Pearson

Showing results (151-160 of 211) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1994
Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditismP Y Fechner, C Rosenberg, G Stetten, et al.
Progress in Clinical and Biological Research|January 1, 1989
Characterization of new probes for diagnosis of polycystic kidney disease (PKD1)M H Breuning, A Verwest, J Ijdo, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridizationT Kievits, J G Dauwerse, J Wiegant, et al.
Human Genetics|August 1, 1990
Somatic origin of inherited haemophilia AA H Bröcker-Vriends, E Briët, J C Dreesen, et al.
Lancet (London, England)|December 12, 1987
Improved early diagnosis of adult polycystic kidney disease with flanking DNA markersM H Breuning, S T Reeders, H Brunner, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 20, 2000
Refined genetic and comparative physical mapping of the canine copper toxicosis locusB van de Sluis, S Kole, M van Wolferen, et al.
Cytogenetics and Cell Genetics|January 1, 1986
Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21P Devilee, T Cremer, P Slagboom, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson's diseaseC Wijmenga, T Müller, I S Murli, et al.
Human Genetics|February 1, 1987
Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletionsM Mannens, R M Slater, C Heyting, et al.
Journal of Medical Genetics|December 1, 1986
DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedureE Bakker, E J Bonten, L F De Lange, et al.
Pageof 22

Showing results (151-160 of 211) with videos related to

Sort By:
Pageof 22
Cytogenetics and Cell Genetics|January 1, 1994
Nonrandom inactivation of the Y-bearing X chromosome in a 46,XX individual: evidence for the etiology of 46,XX true hermaphroditismP Y Fechner, C Rosenberg, G Stetten, et al.
Progress in Clinical and Biological Research|January 1, 1989
Characterization of new probes for diagnosis of polycystic kidney disease (PKD1)M H Breuning, A Verwest, J Ijdo, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridizationT Kievits, J G Dauwerse, J Wiegant, et al.
Human Genetics|August 1, 1990
Somatic origin of inherited haemophilia AA H Bröcker-Vriends, E Briët, J C Dreesen, et al.
Lancet (London, England)|December 12, 1987
Improved early diagnosis of adult polycystic kidney disease with flanking DNA markersM H Breuning, S T Reeders, H Brunner, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 20, 2000
Refined genetic and comparative physical mapping of the canine copper toxicosis locusB van de Sluis, S Kole, M van Wolferen, et al.
Cytogenetics and Cell Genetics|January 1, 1986
Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21P Devilee, T Cremer, P Slagboom, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson's diseaseC Wijmenga, T Müller, I S Murli, et al.
Human Genetics|February 1, 1987
Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletionsM Mannens, R M Slater, C Heyting, et al.
Journal of Medical Genetics|December 1, 1986
DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedureE Bakker, E J Bonten, L F De Lange, et al.
Pageof 22