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 265
... somatic reassortment 4. Mechanism of action of mutant genes 5. Frequency of occurrence of mutant cells in a cell population a . Spontaneous b . Induced genes . The existence of these two ... somatic cell genetics 1. Somatic cell genetics 265.
... somatic reassortment 4. Mechanism of action of mutant genes 5. Frequency of occurrence of mutant cells in a cell population a . Spontaneous b . Induced genes . The existence of these two ... somatic cell genetics 1. Somatic cell genetics 265.
Seite 268
... somatic cell genetics which will not be apparent from my tabulations . Somatic cell genetics is a field largely populated by amateurs , and for two reasons . First , because the field is young , only a small fraction of the people doing ...
... somatic cell genetics which will not be apparent from my tabulations . Somatic cell genetics is a field largely populated by amateurs , and for two reasons . First , because the field is young , only a small fraction of the people doing ...
Seite 284
... SOMATIC CELL HYBRIDIZATION TO PROBE THE MECHANISMS WHICH MAINTAIN CELL DIFFERENTIATION MARY C. WEISS Centre de Génétique Moléculaire du CNRS , Gif - sur - Yvette , France One of the many applications of somatic cell hybridization has ...
... SOMATIC CELL HYBRIDIZATION TO PROBE THE MECHANISMS WHICH MAINTAIN CELL DIFFERENTIATION MARY C. WEISS Centre de Génétique Moléculaire du CNRS , Gif - sur - Yvette , France One of the many applications of somatic cell hybridization has ...
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