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 51
... origin of the additional chromosome 21 , as illustrated by Case 1 in Table 6 where the conditional probability for all 4 types of origin is shown for every possible type of Down's syndrome . While the mating class in which all 4 ...
... origin of the additional chromosome 21 , as illustrated by Case 1 in Table 6 where the conditional probability for all 4 types of origin is shown for every possible type of Down's syndrome . While the mating class in which all 4 ...
Seite 287
... origin and histogenetic origin . In all three of these cases , extinction of the liver - specific enzymes was observed : activity of tyrosine aminotransferase ( TAT ) , alanine aminotransferase ( AAT ) , aldolase B and alcohol ...
... origin and histogenetic origin . In all three of these cases , extinction of the liver - specific enzymes was observed : activity of tyrosine aminotransferase ( TAT ) , alanine aminotransferase ( AAT ) , aldolase B and alcohol ...
Seite 380
... origin as compared with those who have little pectoral hair ( Müller , 1952 ) . The hair pattern precedes the onset of cirrhosis and appears to be a biologic marker for liver toxicity . The pathophysiology of this association and its ...
... origin as compared with those who have little pectoral hair ( Müller , 1952 ) . The hair pattern precedes the onset of cirrhosis and appears to be a biologic marker for liver toxicity . The pathophysiology of this association and its ...
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