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Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal diagnosis of Duchenne muscular dystrophy: a three-year experience in a rapidly evolving fieldE Bakker, E J Bonten, H Veenema, et al.Human Reproduction (Oxford, England)|April 1, 1997
Intracytoplasmic sperm injection (ICSI) and chromosomally abnormal spermatozoaP A In't Veld, F J Broekmans, H F de France, et al.Cancer Research|October 15, 1988
Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probesP Devilee, R F Thierry, T Kievits, et al.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.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.Pageof 14