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 99
... indicate a pericentric inversion . The sign ( ) indicates acquisition of heterochromatic material . The two chimpanzee chromosomes corresponding to the human 2 have been designated [ 2p ] and [ 2q ] . Autosomal enzymatic markers Table 1 ...
... indicate a pericentric inversion . The sign ( ) indicates acquisition of heterochromatic material . The two chimpanzee chromosomes corresponding to the human 2 have been designated [ 2p ] and [ 2q ] . Autosomal enzymatic markers Table 1 ...
Seite 280
... indicates human chromosome 17 . A second way to estimate the size of the transgenome is to employ a genetic approach ... indicate that the distance between TK and GalK in man is no more than 0.001 of the haploid genome , or 1-3 x 106 nbp ...
... indicates human chromosome 17 . A second way to estimate the size of the transgenome is to employ a genetic approach ... indicate that the distance between TK and GalK in man is no more than 0.001 of the haploid genome , or 1-3 x 106 nbp ...
Seite 319
... indicate that the two Class I loci are homologous and most likely arose by gene duplication ( for a discussion , see Klein , 1976 ) . In fact , the products of these two loci are so similar to one another in their amino acid sequence ...
... indicate that the two Class I loci are homologous and most likely arose by gene duplication ( for a discussion , see Klein , 1976 ) . In fact , the products of these two loci are so similar to one another in their amino acid sequence ...
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