Showing results (191-200 of 285) with videos related to

Sort By:
Pageof 29
Blood|November 15, 1996
A combination of the effects of rare genotypes at the XK and KEL blood group loci results in absence of Kell system antigens from the red blood cellsG L Daniels, F Weinauer, C Stone, et al.
Transplantation|February 1, 1989
Sequential determinations of urinary cytology and plasma and urinary lymphokines in the management of renal allograft recipientsM A Simpson, P N Madras, A J Cornaby, et al.
Transplantation|November 1, 1991
The effect of antilymphocyte serum, fractionated donor bone marrow, and cyclosporine on renal allograft survival in mongrel dogsW C Hartner, T G Markees, S R De Fazio, et al.
Genomics|March 1, 1997
A gene-based genetic linkage and comparative map of the rat X chromosomeI Y Millwood, M T Bihoreau, D Gauguier, et al.
International Journal of Cancer|March 15, 1975
Activation of C-type viruses during skin graft rejection in the mouse. Interrelationships between immunostimulation and immunosuppressionM S Hirsch, D A Ellis, A P Kelly, et al.
Journal of Medical Genetics|March 1, 1994
X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphismsS Cochrane, J Bergoffen, N D Fairweather, et al.
Genomics|January 27, 1998
Two members of the human MAGEB gene family located in Xp21.3 are expressed in tumors of various histological originsC Lurquin, C De Smet, F Brasseur, et al.
American Journal of Medical Genetics|September 22, 1999
Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism ConsortiumE Maestrini, C Lai, A Marlow, et al.
The Journal of Bone and Joint Surgery. British Volume|September 28, 2004
Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype studyD E Porter, L Lonie, M Fraser, et al.
Human Molecular Genetics|August 1, 1997
Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 geneY Ishikawa-Brush, J F Powell, P Bolton, et al.
Pageof 29