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 64
... culture . However , the patterns of chromosomal aberrations observed in the two disorders differ , being distinctive ... Cultures of cells from both the heterozygote and the homozygote usually show increased numbers of aberrations ...
... culture . However , the patterns of chromosomal aberrations observed in the two disorders differ , being distinctive ... Cultures of cells from both the heterozygote and the homozygote usually show increased numbers of aberrations ...
Seite 191
... culture , or it is possible that it is present in extra embryonic tissues in vivo . Cox et al . ( 1974 ) suggested a method which may assist in the interpretation of a mosaic culture . These authors utilized the analysis of colonies ...
... culture , or it is possible that it is present in extra embryonic tissues in vivo . Cox et al . ( 1974 ) suggested a method which may assist in the interpretation of a mosaic culture . These authors utilized the analysis of colonies ...
Seite 394
... culture historical hypothesis ' for the contention that lactose absorbers enjoyed a nutritional advantage after the initiation of the milking habit in pastoral groups in the neolithic era ( 7-8000 years ago ) . Although there is no ...
... culture historical hypothesis ' for the contention that lactose absorbers enjoyed a nutritional advantage after the initiation of the milking habit in pastoral groups in the neolithic era ( 7-8000 years ago ) . Although there is no ...
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