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 191
... relatively high frequency of both numerical and structural chromosome mosaicism in amniotic fluid cultures may complicate the interpretation of the chromosome findings . Table 7 indicates that only in a few instances does chromosome ...
... relatively high frequency of both numerical and structural chromosome mosaicism in amniotic fluid cultures may complicate the interpretation of the chromosome findings . Table 7 indicates that only in a few instances does chromosome ...
Seite 196
... relatively small number of prenatal biochemical analyses ( Galjaard , 1976 ) . This is especially true for Great Britain and West Germany where 11 and 12 centres performed about 100 and 30 prenatal enzyme analyses respectively . During ...
... relatively small number of prenatal biochemical analyses ( Galjaard , 1976 ) . This is especially true for Great Britain and West Germany where 11 and 12 centres performed about 100 and 30 prenatal enzyme analyses respectively . During ...
Seite 207
... relatively short period of time , the potential of intrauterine diagnosis , as predicted by Ballantyne in 1902 , has been thoroughly documented . Numerous reviews of antenatal detection have been published within the past few years ...
... relatively short period of time , the potential of intrauterine diagnosis , as predicted by Ballantyne in 1902 , has been thoroughly documented . Numerous reviews of antenatal detection have been published within the past few years ...
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