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 38
... genes relatively specific in their action ? 2. How are these units organized in the genome ; are there common patterns of organization ? How are temporal genes organized relative to each other and to the structural gene they program ...
... genes relatively specific in their action ? 2. How are these units organized in the genome ; are there common patterns of organization ? How are temporal genes organized relative to each other and to the structural gene they program ...
Seite 39
... gene , and presumably analogous to the glucuronidase temporal gene . The a - galactosidase , ß - galactosidase and amylase systems tell us that separate DNA sequences are involved in programming structural genes during development , and ...
... gene , and presumably analogous to the glucuronidase temporal gene . The a - galactosidase , ß - galactosidase and amylase systems tell us that separate DNA sequences are involved in programming structural genes during development , and ...
Seite 40
... gene further down on the X chromosome . Tem also has 2 alleles , early and late , which cause respectively the early and late expression of the H2 antigen . The H2 system thus introduces a new element into our conception of temporal genes ...
... gene further down on the X chromosome . Tem also has 2 alleles , early and late , which cause respectively the early and late expression of the H2 antigen . The H2 system thus introduces a new element into our conception of temporal genes ...
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