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 172
... maternal serum levels of AFP in CNS malformations have been studied and it now seems that approximately 90 % of cases of anencephaly and 50 % of cases of open spina bifida are associated with raised maternal serum levels of AFP ...
... maternal serum levels of AFP in CNS malformations have been studied and it now seems that approximately 90 % of cases of anencephaly and 50 % of cases of open spina bifida are associated with raised maternal serum levels of AFP ...
Seite 183
... maternal ages . among 1769 newborn infants whose mothers were 35 years obtained from newborn chromosome screening surveys ( Table 6 ) ( Lubs , personal communication ) . Mosaicism The interpretation of chromosome mosaicism in amniotic ...
... maternal ages . among 1769 newborn infants whose mothers were 35 years obtained from newborn chromosome screening surveys ( Table 6 ) ( Lubs , personal communication ) . Mosaicism The interpretation of chromosome mosaicism in amniotic ...
Seite 188
... maternal age or the birth of a previous child with a chromosome abnormality , usually in the same sibship ( Table 1 ) . Over 90 % of amniocenteses in this latter category were indicated because of the birth of a previous sib with 21 ...
... maternal age or the birth of a previous child with a chromosome abnormality , usually in the same sibship ( Table 1 ) . Over 90 % of amniocenteses in this latter category were indicated because of the birth of a previous sib with 21 ...
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