Showing results (21-30 of 4,303) with videos related to
Sort By:
Pageof 431
American Journal of Hematology|January 1, 1977
Isozyme patterns in erythrocytes from human fetusesS H Chen, J E Anderson, E R Giblett, et al.The Journal of Pediatrics|March 1, 1978
A new form of nucleoside phosphorylase deficiency in two brothers with defective T-cell functionW D Biggar, E R Giblett, R L Ozere, et al.Biochemical Genetics|February 1, 1983
Polymorphism of the sixth component of complement (C6) in the dogJ E Anderson, W C Ladiges, E R Giblett, et al.Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|January 1, 1976
Hereditary retinoschisis linkage studies in a family and considerations in genetic counsellingH Boman, P Heilig, H E Kolder, et al.Transplantation|December 1, 1978
Immunoglobulin production of donor origin after marrow transplantation for acute leukemia or aplastic anemiaR P Witherspoon, M S Schanfield, R Storb, et al.Journal of Medical Genetics|October 1, 1980
Clinical manifestations of familial 13;18 translocationW A Blattner, M L Kistenmacher, S Tsai, et al.Lancet (London, England)|May 3, 1975
Nucleoside-phosphorylase deficiency in a child with severely defective T-cell immunity and normal B-cell immunityE R Giblett, A J Ammann, D W Wara, et al.The Journal of Pediatrics|November 1, 1980
Detection of heterozygotes for congenital adrenal hyperplasia: 21-hydroxylase deficiency-a comparison of HLA typing and 17-OH progesterone response to ACTH infusionR S Mauseth, J A Hansen, E K Smith, et al.The Journal of Clinical Investigation|December 1, 1978
Adenosine deaminase deficiency: disappearance of adenine deoxynucleotides from a patient's erythrocytes after successful marrow transplantationS H Chen, H D Ochs, C R Scott, et al.American Journal of Human Genetics|May 1, 1983
Plasma paraoxonase polymorphism: a new enzyme assay, population, family, biochemical, and linkage studiesR F Mueller, S Hornung, C E Furlong, et al.Pageof 431