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
... suggested that this may not be true and that mothers referred for amniocentesis may often be selected by themselves or their obstetricians because of a poor obstetric or family history or because of other factors in the parental medical ...
... suggested that this may not be true and that mothers referred for amniocentesis may often be selected by themselves or their obstetricians because of a poor obstetric or family history or because of other factors in the parental medical ...
Seite 343
... suggested by an approximately 20 % rate of concordance in identical twins ( Miller , 1971 ) . The limited data for other cancers suggest no clear excess concordance in identical twins ( Anderson , 1975 ) . Evidence for a genetic ...
... suggested by an approximately 20 % rate of concordance in identical twins ( Miller , 1971 ) . The limited data for other cancers suggest no clear excess concordance in identical twins ( Anderson , 1975 ) . Evidence for a genetic ...
Seite 380
... suggested that vasodilatation is caused by acetaldehyde . Slower rates of alcohol breakdown said to occur in Indians ... suggest that pathologic addiction to alcohol - alcoholism has genetic determinants of an unspecified nature ...
... suggested that vasodilatation is caused by acetaldehyde . Slower rates of alcohol breakdown said to occur in Indians ... suggest that pathologic addiction to alcohol - alcoholism has genetic determinants of an unspecified nature ...
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