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 183
... Table 1 together with the numbers of affected fetuses found in each group . Tables 2 , 3 , and 4 summarize the chromosome findings observed among affected fetuses for each major indication . Table 5 summarizes the age - specific ...
... Table 1 together with the numbers of affected fetuses found in each group . Tables 2 , 3 , and 4 summarize the chromosome findings observed among affected fetuses for each major indication . Table 5 summarizes the age - specific ...
Seite 265
... TABLE 2 Kinds of information so far obtained about specified loci 1. Dominance relations 2. Genetic complementation 3. Synteny and somatic reassortment 4. Mechanism of action of mutant genes 5. Frequency of occurrence of mutant cells in ...
... TABLE 2 Kinds of information so far obtained about specified loci 1. Dominance relations 2. Genetic complementation 3. Synteny and somatic reassortment 4. Mechanism of action of mutant genes 5. Frequency of occurrence of mutant cells in ...
Seite 312
... Table 2 ) . 3 Cell negative for BW35 but carried highly cross- reactive group HR . TABLE 4 Example of killing of a non - HLA coded target in family Ref . Responder ( sensitizer ) Killing function of siblings ? Sensitizing haplotype1 C1 ...
... Table 2 ) . 3 Cell negative for BW35 but carried highly cross- reactive group HR . TABLE 4 Example of killing of a non - HLA coded target in family Ref . Responder ( sensitizer ) Killing function of siblings ? Sensitizing haplotype1 C1 ...
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