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 127
... region are manifested in particular phenotypes . By means of band analysis , 2 regions can be distinguished on the long arm of chromosome 21 : a proximal region 21q11 → 21q21 , pale in the R and T bands and fluorescent in the Q bands ...
... region are manifested in particular phenotypes . By means of band analysis , 2 regions can be distinguished on the long arm of chromosome 21 : a proximal region 21q11 → 21q21 , pale in the R and T bands and fluorescent in the Q bands ...
Seite 159
... region of embryonic tissue during early embryonic development . The development of any given point of an embryonic field depends on its relations with the other points in its neighborhood or on its position within the region as a whole ...
... region of embryonic tissue during early embryonic development . The development of any given point of an embryonic field depends on its relations with the other points in its neighborhood or on its position within the region as a whole ...
Seite 305
... region within the H - 2 and HLA systems may have some analogies with the immunoglobulin constant heavy chain regions . The relationship of the A , B , C , D and la products to the complement components coded for by genes in the HLA region ...
... region within the H - 2 and HLA systems may have some analogies with the immunoglobulin constant heavy chain regions . The relationship of the A , B , C , D and la products to the complement components coded for by genes in the HLA region ...
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