Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
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Seite 45
... techniques of human chromosomes were available and the implications of these discoveries for human genetics were just beginning to be appreciated . Now , after 5 years experience , I would like to review the impact and utility of ...
... techniques of human chromosomes were available and the implications of these discoveries for human genetics were just beginning to be appreciated . Now , after 5 years experience , I would like to review the impact and utility of ...
Seite 46
... techniques in population surveys Population Total Structural abnormalities examined detected by non - banding G - banding Phenotypically normal newborn babies 619 1 1 Phenotypically abnormal newborn babies Mentally retarded children 204 ...
... techniques in population surveys Population Total Structural abnormalities examined detected by non - banding G - banding Phenotypically normal newborn babies 619 1 1 Phenotypically abnormal newborn babies Mentally retarded children 204 ...
Seite 167
... techniques available for studying the fetus in utero are summarised in Table 1. Of these various techniques the approach most widely adopted is the study of amniotic fluid and the cells contained in it by transabdominal amniocentesis ...
... techniques available for studying the fetus in utero are summarised in Table 1. Of these various techniques the approach most widely adopted is the study of amniotic fluid and the cells contained in it by transabdominal amniocentesis ...
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