Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
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Seite 194
... pregnancies at risk for a metabolic disease ( Table 1 ) . At the end of 1974 206 pregnancies in this category were monitored and 53 foetuses were found to be affected . Prenatal analyses were made for 25 different inborn errors of ...
... pregnancies at risk for a metabolic disease ( Table 1 ) . At the end of 1974 206 pregnancies in this category were monitored and 53 foetuses were found to be affected . Prenatal analyses were made for 25 different inborn errors of ...
Seite 195
... pregnancies at risk monitored in 40 centres in Western Europe ( end 1974 ) No. pregnancies No. affected Chromosomal aberrations Prenatal sex determinations Open neural tube defects Genetic metabolic diseases tested foetuses 4206 280 ...
... pregnancies at risk monitored in 40 centres in Western Europe ( end 1974 ) No. pregnancies No. affected Chromosomal aberrations Prenatal sex determinations Open neural tube defects Genetic metabolic diseases tested foetuses 4206 280 ...
Seite 207
... pregnancies . In most cases , multiple pregnancies are not recognized early in gestation and only one amniotic sac is sampled during amniocentesis . Ultrasonic localization of the placenta presently is being used in most centers prior ...
... pregnancies . In most cases , multiple pregnancies are not recognized early in gestation and only one amniotic sac is sampled during amniocentesis . Ultrasonic localization of the placenta presently is being used in most centers prior ...
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