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 36
... determined by separate DNA sequences , the evidence presented to this point does not rule out the possibility that both of these phenotypes are determined by the same DNA sequence . This last notion implies that the amino acid sequence ...
... determined by separate DNA sequences , the evidence presented to this point does not rule out the possibility that both of these phenotypes are determined by the same DNA sequence . This last notion implies that the amino acid sequence ...
Seite 51
... determining the exact origin of the additional chromosome 21 , as illustrated by Case 1 in Table 6 where the ... determine whether the extra chromosome was maternal or paternal in origin and whether non - disjunction occurred in the ...
... determining the exact origin of the additional chromosome 21 , as illustrated by Case 1 in Table 6 where the ... determine whether the extra chromosome was maternal or paternal in origin and whether non - disjunction occurred in the ...
Seite 291
... determined . somatic cell are nevertheless in a state susceptible to activation . If activation occurs in the absence of reprograming of the responding genome ( in other words , without loss of the original determination , as appears to ...
... determined . somatic cell are nevertheless in a state susceptible to activation . If activation occurs in the absence of reprograming of the responding genome ( in other words , without loss of the original determination , as appears to ...
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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Häufige Begriffe und Wortgruppen
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