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 160
... caused by several different teratogens . Thus , a constellation of more or less regional anomalies , say the Poland ... cause may be associated with greater or lesser disturbance of a field or part of the field ; the results are ...
... caused by several different teratogens . Thus , a constellation of more or less regional anomalies , say the Poland ... cause may be associated with greater or lesser disturbance of a field or part of the field ; the results are ...
Seite 161
... cause ) , a distinction frequently obscured in English biomedical writings . The progress from the stage of the physical examination syndrome to that of the ' pathogenetically defined ' or formal genesis syndrome to the causally defined ...
... cause ) , a distinction frequently obscured in English biomedical writings . The progress from the stage of the physical examination syndrome to that of the ' pathogenetically defined ' or formal genesis syndrome to the causally defined ...
Seite 379
... causing elevations in blood lipids : familial hypercholesterolemia , hereditary hypertriglyceridemia and familial ... cause of myocardial infarction has increased in frequency . only in the last 30-50 years ( Stamler , 1973 ) and is ...
... causing elevations in blood lipids : familial hypercholesterolemia , hereditary hypertriglyceridemia and familial ... cause of myocardial infarction has increased in frequency . only in the last 30-50 years ( Stamler , 1973 ) and is ...
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