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 171
... amniotic fluid cells , antenatal diagnosis might be possible through linkage with a marker trait expressed in amniotic fluid or its cells . So far the known linkage between the loci for secretor status and myotonic dystrophy has been ...
... amniotic fluid cells , antenatal diagnosis might be possible through linkage with a marker trait expressed in amniotic fluid or its cells . So far the known linkage between the loci for secretor status and myotonic dystrophy has been ...
Seite 179
... amniotic fluid and maternal serum drawn prior to amniocentesis ) and in which no explanation even after autopsy of the normal fetus was forthcoming . ( There is evidence that suggests a disorder of the fetus in this case , which will be ...
... amniotic fluid and maternal serum drawn prior to amniocentesis ) and in which no explanation even after autopsy of the normal fetus was forthcoming . ( There is evidence that suggests a disorder of the fetus in this case , which will be ...
Seite 191
... amniotic fluid cultures The finding of a relatively high frequency of both numerical and structural chromosome mosaicism in amniotic fluid cultures may complicate the interpretation of the chromosome findings . Table 7 indicates that ...
... amniotic fluid cultures The finding of a relatively high frequency of both numerical and structural chromosome mosaicism in amniotic fluid cultures may complicate the interpretation of the chromosome findings . Table 7 indicates that ...
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