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 142
... errors of metabolism which include the vitamin - responsive hereditary metabolic diseases ; and the inborn errors of membrane transport which can be seen to accommodate also , abnormalities of the cellular process known as absorptive ...
... errors of metabolism which include the vitamin - responsive hereditary metabolic diseases ; and the inborn errors of membrane transport which can be seen to accommodate also , abnormalities of the cellular process known as absorptive ...
Seite 188
... Errors in chromosome diagnosis These are summarized in Table 8 for 3315 pregnancies monitored in 7 series , giving an error rate of 0.30 % or 1 : 332 amniocenteses . 8 of these errors ( 0.24 % ) resulted from the incorrect determination ...
... Errors in chromosome diagnosis These are summarized in Table 8 for 3315 pregnancies monitored in 7 series , giving an error rate of 0.30 % or 1 : 332 amniocenteses . 8 of these errors ( 0.24 % ) resulted from the incorrect determination ...
Seite 192
... Errors in chromosome diagnosis An error rate of 3 : 1000 amniocenteses , while still too high for satisfaction , indicates a fairly high degree of reliability for the test . The major source of error in the series summarized in Table 8 ...
... Errors in chromosome diagnosis An error rate of 3 : 1000 amniocenteses , while still too high for satisfaction , indicates a fairly high degree of reliability for the test . The major source of error in the series summarized in Table 8 ...
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