Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
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Seite 145
... complex ( Kaufman , 1976 ) . Oxygen and L - phenylalanine interact with a coenzyme , the natural form of which is tetrahydrobiopterin , to permit the parahydroxylation reaction which yields tyrosine . The apoprotein catalyzing this ...
... complex ( Kaufman , 1976 ) . Oxygen and L - phenylalanine interact with a coenzyme , the natural form of which is tetrahydrobiopterin , to permit the parahydroxylation reaction which yields tyrosine . The apoprotein catalyzing this ...
Seite 319
... complex , which codes for thymus - leukemia antigens , is probably related to H - 2 and , in fact , were it not for historical reasons , would have to be considered a part of the H - 2 complex . On the same side , at a distance of some ...
... complex , which codes for thymus - leukemia antigens , is probably related to H - 2 and , in fact , were it not for historical reasons , would have to be considered a part of the H - 2 complex . On the same side , at a distance of some ...
Seite 325
... COMPLEX AND CELL - MEDIATED IMMUNITY * ROLF M. ZINKERNAGEL Department of Cellular and Developmental Immunology , Scripps Clinic and Research Foundation , La Jolla , Calif . , U.S.A. In mice , all known functions mediated by thymus ...
... COMPLEX AND CELL - MEDIATED IMMUNITY * ROLF M. ZINKERNAGEL Department of Cellular and Developmental Immunology , Scripps Clinic and Research Foundation , La Jolla , Calif . , U.S.A. In mice , all known functions mediated by thymus ...
Inhalt
The legal aspects of genetic screening and counseling | 3 |
Some trends in the study of spontaneous and induced mutation in | 19 |
Temporal genes and developmental programs | 33 |
Urheberrecht | |
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aberrations Acad activity alleles Amer amniocentesis amniotic fluid amniotic fluid cells analysis antenatal antigens assay autosomal banding biochemical blood group Bodmer cancer cell hybridization chromatid chromosome abnormalities clinical clones congenital correlation culture cytogenetic deficiency detected determined differentiation disease disorders donor Down's syndrome Editors environmental enzyme errors of metabolism extinction factors fetal fetus fibroblasts frequency functions Galjaard gene genetic distance genome H-2 complex hemoglobin HLA-D Human Genetics inborn errors individuals inheritance involved karyotype lactose Lancet linkage disequilibrium loci locus lymphocytes malformations marker maternal methods microcell Milunsky mouse mutagens mutation rates Nature Lond neural tube defects newborns normal observed parents patients phenotype phenylketonuria polymorphism population genetics possible pregnancies prenatal diagnosis Press Proc protein recent risk Ruddle samples selection somatic cell specific structural studies suggested Table techniques tissue translocation tumors variants X chromosome Zinkernagel