Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
Ergebnisse 1-3 von 46
Seite 8
... parents won the right to sue 2 physicians for their alleged failure to inform them of the risk of congenital defects inherent in another pregnancy . The parents alleged that the obstetricians had said there was no reason to fear that a ...
... parents won the right to sue 2 physicians for their alleged failure to inform them of the risk of congenital defects inherent in another pregnancy . The parents alleged that the obstetricians had said there was no reason to fear that a ...
Seite 10
... parents , as well as the doctor , must share the blame for genetically defective children . The ultimate question becomes this : is the right of the parent ( s ) to reproduce paramount to the right of the child to be born physically and ...
... parents , as well as the doctor , must share the blame for genetically defective children . The ultimate question becomes this : is the right of the parent ( s ) to reproduce paramount to the right of the child to be born physically and ...
Seite 194
... parents are not aware of the 1 in 4 recurrence risk when they have subsequent pregnancies . In too many instances clinicians do not inform parents about the high recurrence risk even if it has been demonstrated that one of their ...
... parents are not aware of the 1 in 4 recurrence risk when they have subsequent pregnancies . In too many instances clinicians do not inform parents about the high recurrence risk even if it has been demonstrated that one of their ...
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