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 65
... disorders , BS , FA , LBS , and XP , clones with a visible . mutation in chromosome complement have been detected in circulating lymphocytes or cultured fibroblasts . Although the clones have with one exception ( McCaw et al . , 1975 ) ...
... disorders , BS , FA , LBS , and XP , clones with a visible . mutation in chromosome complement have been detected in circulating lymphocytes or cultured fibroblasts . Although the clones have with one exception ( McCaw et al . , 1975 ) ...
Seite 195
... disorders , genetic counseling and education of medical and social workers and the general public on the possibilities of postnatal and prenatal diagnosis . To inspire confidence in prenatal monitoring the quality of the analyses should ...
... disorders , genetic counseling and education of medical and social workers and the general public on the possibilities of postnatal and prenatal diagnosis . To inspire confidence in prenatal monitoring the quality of the analyses should ...
Seite 207
... disorders dealt with the determination of fetal sex in pregnancies at risk for X - linked recessive disorders . Shortly thereafter , successful cultivation of amniotic fluid cells permitted the detection of Down's syndrome , other ...
... disorders dealt with the determination of fetal sex in pregnancies at risk for X - linked recessive disorders . Shortly thereafter , successful cultivation of amniotic fluid cells permitted the detection of Down's syndrome , other ...
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