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 189
... risk for a chromosome abnormality in their fetus over and above the maternal age factor ; ( 2 ) the newborn surveys may be biased to give a lower frequency of chromosome abnormalities than the true population incidence , or ...
... risk for a chromosome abnormality in their fetus over and above the maternal age factor ; ( 2 ) the newborn surveys may be biased to give a lower frequency of chromosome abnormalities than the true population incidence , or ...
Seite 194
... risk of having another child with a genetic disease the metabolic defect of which could be expressed in cultured amniotic fluid cells . There are several reasons why only a small percentage of parents at risk are referred for prenatal ...
... risk of having another child with a genetic disease the metabolic defect of which could be expressed in cultured amniotic fluid cells . There are several reasons why only a small percentage of parents at risk are referred for prenatal ...
Seite 341
... risk factors . It is estimated that already known environmental stimuli may be responsible for about 30-40 % of common cancers in Western societies ( Higginson , 1976 ) . These risk factors spelled out in a recent review ( Fraumeni ...
... risk factors . It is estimated that already known environmental stimuli may be responsible for about 30-40 % of common cancers in Western societies ( Higginson , 1976 ) . These risk factors spelled out in a recent review ( Fraumeni ...
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