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 22
... mutation on some of the proteins one might study hemoglobin , albumin , carbonic anhydrase , transferrin and given the universality of the genetic code , the study of mutation moves to a new plane in higher organisms , a plane vital to ...
... mutation on some of the proteins one might study hemoglobin , albumin , carbonic anhydrase , transferrin and given the universality of the genetic code , the study of mutation moves to a new plane in higher organisms , a plane vital to ...
Seite 25
... mutation is non - repetitive ; ( 3 ) each electrophoretic class defines only one variant ; and ( 4 ) the population is in equilibrium as regards mutation , 0 = 4Neμ = ( 3 ) where Ne effective population number and μ = mutation rate ...
... mutation is non - repetitive ; ( 3 ) each electrophoretic class defines only one variant ; and ( 4 ) the population is in equilibrium as regards mutation , 0 = 4Neμ = ( 3 ) where Ne effective population number and μ = mutation rate ...
Seite 28
... mutation rate therefore 5 x 107 x 102 x 0.5 = 2.5 x 10-9 / nucleotide / generation . - became Kimura and Ohta's estimate , based on the extensive screenings for hemoglobin variants carried out by Japanese investigators , was for the ...
... mutation rate therefore 5 x 107 x 102 x 0.5 = 2.5 x 10-9 / nucleotide / generation . - became Kimura and Ohta's estimate , based on the extensive screenings for hemoglobin variants carried out by Japanese investigators , was for the ...
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