Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
Ergebnisse 1-3 von 38
Seite 72
... reported in which the rearrangement involved 3 chromosomes ; in all of these cases , with one possible exception ( Ishihara et al . , 1974 ) , 2 of the chromosomes were Nos . 9 and 22 with breaks in the usual band ( Engel et al . , 1974 ...
... reported in which the rearrangement involved 3 chromosomes ; in all of these cases , with one possible exception ( Ishihara et al . , 1974 ) , 2 of the chromosomes were Nos . 9 and 22 with breaks in the usual band ( Engel et al . , 1974 ...
Seite 176
... reported elsewhere . The first 5,000 cases are summarized in Table 1. Note that the recurrence of a neural tube defect in a couple with 1 previously affected child was only 1.5 % in contrast to higher rates of recurrence reported in ...
... reported elsewhere . The first 5,000 cases are summarized in Table 1. Note that the recurrence of a neural tube defect in a couple with 1 previously affected child was only 1.5 % in contrast to higher rates of recurrence reported in ...
Seite 212
... reported the successful aspiration of an anterior placenta in 11 of 19 cases studied . In these 11 cases , fetal red cells comprised 2-95 % of the mixtures . Mixtures of only 5 % fetal cells previously have been shown to be all that is ...
... reported the successful aspiration of an anterior placenta in 11 of 19 cases studied . In these 11 cases , fetal red cells comprised 2-95 % of the mixtures . Mixtures of only 5 % fetal cells previously have been shown to be all that 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 | |
30 weitere Abschnitte werden nicht angezeigt.
Andere Ausgaben - Alle anzeigen
Häufige Begriffe und Wortgruppen
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