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 40
... expression of the adjacent H2 region on chromosome 17. There are 2 alleles of Rec also , A and B. Rec is capable of ... expressed . Finally , we have no information as to whether programmatic controls can involve changes in DNA sequence ...
... expression of the adjacent H2 region on chromosome 17. There are 2 alleles of Rec also , A and B. Rec is capable of ... expressed . Finally , we have no information as to whether programmatic controls can involve changes in DNA sequence ...
Seite 291
... expressed in a determined . somatic cell are nevertheless in a state susceptible to activation . If activation occurs in the absence of reprograming of the responding genome ( in other words , without loss of the original determination ...
... expressed in a determined . somatic cell are nevertheless in a state susceptible to activation . If activation occurs in the absence of reprograming of the responding genome ( in other words , without loss of the original determination ...
Seite 331
... expressed receptors . This model is easily compatible with all available data stemming from analysis of the specificity of cytotoxic T cells generated during virus infections , the activity against minor histocompatibility antigens or ...
... expressed receptors . This model is easily compatible with all available data stemming from analysis of the specificity of cytotoxic T cells generated during virus infections , the activity against minor histocompatibility antigens or ...
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