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American Journal of Medical Genetics|September 12, 2000
Rapid screening method to detect mutations in CYP21, the gene for 21-hydroxylaseY Yokoyama, M Teraoka, K Tsuji, et al.
Bone Marrow Transplantation|October 1, 1994
Change of serum alpha-1 microglobulin and beta-2 microglobulin following allogeneic bone marrow transplantationT Ashida, K Tsubaki, F Urase, et al.
Journal of Medical Genetics|June 1, 1992
Terminal 22q deletion associated with a partial deficiency of arylsulphatase AK Narahara, Y Takahashi, M Murakami, et al.
American Journal of Nephrology|January 1, 1984
IgA nephropathy associated with HLA-DR4 antigenY Nomoto, M Endoh, M Miura, et al.
American Journal of Medical Genetics|August 26, 1998
45,X/46,X,idic(Yq) mosaicism: clinical, cytogenetic, and molecular studies in four individualsM Teraoka, K Narahara, Y Yokoyama, et al.
Radioisotopes|July 1, 1979
[In vivo distributions of 111In and/or 3H labeled lymphocyte in C3H/He mouse (author's transl)]C Shibata, Y Shiwaku, Y Ohizumi, et al.
Clinical and Experimental Rheumatology|July 1, 1986
Familial Sjögren's syndrome in the Japanese: immunogenetic and serological studiesJ Moriuchi, Y Ichikawa, M Takaya, et al.
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