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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 segment
Y 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-cen
V 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 lethality
W 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 electrophoresis
T 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 dystrophy
I van Bakel, S Holt, I Craig, et al.
Cureus
|
February 17, 2026
Depression and Resilience in Youth Mixed Martial Arts Athletes: A Cross-Sectional Analysis
Jeffrey 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 repeat
S H Laval, V Reed, H J Blair, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 29, 1999
Mouse X chromosome
Y Boyd, P Denny, W Masson, et al.
Genomics
|
July 1, 1989
Localization of the properdin structural locus to Xp11.23-Xp21.1
D 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 disease
W Masson, H Hughes, D Papworth, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 95) with videos related to
Sort By:
Page
of 10
Immunogenetics
|
February 28, 2001
Mapping of the chicken and mouse genes for toll-like receptor 2 (TLR2) to an evolutionarily conserved chromosomal segment
Y 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-cen
V 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 lethality
W 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 electrophoresis
T 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 dystrophy
I van Bakel, S Holt, I Craig, et al.
Cureus
|
February 17, 2026
Depression and Resilience in Youth Mixed Martial Arts Athletes: A Cross-Sectional Analysis
Jeffrey 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 repeat
S H Laval, V Reed, H J Blair, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 29, 1999
Mouse X chromosome
Y Boyd, P Denny, W Masson, et al.
Genomics
|
July 1, 1989
Localization of the properdin structural locus to Xp11.23-Xp21.1
D 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 disease
W Masson, H Hughes, D Papworth, et al.
Page
of 10