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 149
... possible example of mutation at the gene locus for the factor required to specify GM2 cleavage activity by the hexosaminidase A isozyme . The other variants can be considered as variations on these three basic themes . While the ...
... possible example of mutation at the gene locus for the factor required to specify GM2 cleavage activity by the hexosaminidase A isozyme . The other variants can be considered as variations on these three basic themes . While the ...
Seite 196
... possible in cases where an affected foetus has been detected . The use of microtechniques makes possible biochemical assays with small numbers of cultured cells ( Galjaard et al . , 1973 , 1974a , b ) , and hence reduces the interval ...
... possible in cases where an affected foetus has been detected . The use of microtechniques makes possible biochemical assays with small numbers of cultured cells ( Galjaard et al . , 1973 , 1974a , b ) , and hence reduces the interval ...
Seite 352
... possible non - enzymatic factors that enhance excision of dimers from chromatin ( Mortelmans et al . , 1976 ) , apurinic endonuclease ( Kuhnlein et al . , 1976 ) , and uracil - N - glycosidase ( Cook and Friedberg , unpublished ...
... possible non - enzymatic factors that enhance excision of dimers from chromatin ( Mortelmans et al . , 1976 ) , apurinic endonuclease ( Kuhnlein et al . , 1976 ) , and uracil - N - glycosidase ( Cook and Friedberg , unpublished ...
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