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Y Boyd

Showing results (21-30 of 95) with videos related to

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Immunogenetics|February 28, 2001
Mapping of the chicken and mouse genes for toll-like receptor 2 (TLR2) to an evolutionarily conserved chromosomal segmentY Boyd, M Goodchild, S Morroll, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Partial sequence data from three evolutionarily conserved loci from the proximal short arm of the human X chromosome; assignment of DXF34S1 to Xp11.21-cenV Reed, S Laval, G Maslen, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 1, 1996
The use of compound heterozygotes and Hprt selection to analyze X-linked mottled alleles associated with prenatal lethalityW Masson, S Holt, V Reed, et al.
Genomics|November 1, 1988
Mapping of Xp21 translocation breakpoints in and around the DMD gene by pulsed field gel electrophoresisT Meitinger, Y Boyd, R Anand, et al.
American Journal of Human Genetics|August 1, 1995
Sequence analysis of the breakpoint regions of an X;5 translocation in a female with Duchenne muscular dystrophyI van Bakel, S Holt, I Craig, et al.
Cureus|February 17, 2026
Depression and Resilience in Youth Mixed Martial Arts Athletes: A Cross-Sectional AnalysisJeffrey Fujimoto, Alexandra Y Boyd, Karen Ladnier, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1997
The structure of DXF34, a human X-linked sequence family with homology to a transcribed mouse Y-linked repeatS H Laval, V Reed, H J Blair, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 1999
Mouse X chromosomeY Boyd, P Denny, W Masson, et al.
Genomics|July 1, 1989
Localization of the properdin structural locus to Xp11.23-Xp21.1D Goundis, S M Holt, Y Boyd, et al.
Journal of Medical Genetics|October 10, 1997
Abnormalities of copper accumulation in cell lines established from nine different alleles of mottled are the same as those found in Menkes diseaseW Masson, H Hughes, D Papworth, et al.
Pageof 10

Showing results (21-30 of 95) with videos related to

Sort By:
Pageof 10
Immunogenetics|February 28, 2001
Mapping of the chicken and mouse genes for toll-like receptor 2 (TLR2) to an evolutionarily conserved chromosomal segmentY Boyd, M Goodchild, S Morroll, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Partial sequence data from three evolutionarily conserved loci from the proximal short arm of the human X chromosome; assignment of DXF34S1 to Xp11.21-cenV Reed, S Laval, G Maslen, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 1, 1996
The use of compound heterozygotes and Hprt selection to analyze X-linked mottled alleles associated with prenatal lethalityW Masson, S Holt, V Reed, et al.
Genomics|November 1, 1988
Mapping of Xp21 translocation breakpoints in and around the DMD gene by pulsed field gel electrophoresisT Meitinger, Y Boyd, R Anand, et al.
American Journal of Human Genetics|August 1, 1995
Sequence analysis of the breakpoint regions of an X;5 translocation in a female with Duchenne muscular dystrophyI van Bakel, S Holt, I Craig, et al.
Cureus|February 17, 2026
Depression and Resilience in Youth Mixed Martial Arts Athletes: A Cross-Sectional AnalysisJeffrey Fujimoto, Alexandra Y Boyd, Karen Ladnier, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1997
The structure of DXF34, a human X-linked sequence family with homology to a transcribed mouse Y-linked repeatS H Laval, V Reed, H J Blair, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 1999
Mouse X chromosomeY Boyd, P Denny, W Masson, et al.
Genomics|July 1, 1989
Localization of the properdin structural locus to Xp11.23-Xp21.1D Goundis, S M Holt, Y Boyd, et al.
Journal of Medical Genetics|October 10, 1997
Abnormalities of copper accumulation in cell lines established from nine different alleles of mottled are the same as those found in Menkes diseaseW Masson, H Hughes, D Papworth, et al.
Pageof 10