Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
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Seite 118
... Lymphocytes Fibroblasts 74 3 97 107 19 17 966 36 3 28 35 Case 2 Lymphocytes 10 10 175 2 197 32 6 38 Fibroblasts 5 2 15 22 Case 3 Lymphocytes 2 52 54 Case 4 Lymphocytes 2 1 84 1 88 12 12 Case 5 Lymphocytes 3 4 146 153 12 1 13 The X ...
... Lymphocytes Fibroblasts 74 3 97 107 19 17 966 36 3 28 35 Case 2 Lymphocytes 10 10 175 2 197 32 6 38 Fibroblasts 5 2 15 22 Case 3 Lymphocytes 2 52 54 Case 4 Lymphocytes 2 1 84 1 88 12 12 Case 5 Lymphocytes 3 4 146 153 12 1 13 The X ...
Seite 300
... lymphocytes and macrophages , though more recent studies have shown the existence of several la loci , including at least one that determines antigenic specificities on a class of T lymphocytes ( McDevitt , 1976 ) . These antigenic ...
... lymphocytes and macrophages , though more recent studies have shown the existence of several la loci , including at least one that determines antigenic specificities on a class of T lymphocytes ( McDevitt , 1976 ) . These antigenic ...
Seite 308
... lymphocyte proliferation and effector stages were represented in part by the specific ability of sensitized lymphocytes to kill target cells . However , it was noted that certain stages of lymphocyte differentiation occurred ...
... lymphocyte proliferation and effector stages were represented in part by the specific ability of sensitized lymphocytes to kill target cells . However , it was noted that certain stages of lymphocyte differentiation occurred ...
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