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 87
... shown that when fixed or unfixed chromatin is spread using formalin it has the appearance of single 20 Å fibres connecting up blobs of protein giving a pearls on a string arrangement ( Fig . 3 ) . This beaded structure is found in ...
... shown that when fixed or unfixed chromatin is spread using formalin it has the appearance of single 20 Å fibres connecting up blobs of protein giving a pearls on a string arrangement ( Fig . 3 ) . This beaded structure is found in ...
Seite 303
... shown a strong linkage disequilibrium between DW2 and B7 and there is a well known relatively strong linkage disequilibrium in caucasian populations between B7 and A3 . Thus , of the three associations shown in the table with multiple ...
... shown a strong linkage disequilibrium between DW2 and B7 and there is a well known relatively strong linkage disequilibrium in caucasian populations between B7 and A3 . Thus , of the three associations shown in the table with multiple ...
Seite 367
... shown us how complicated this question can be . One virus , SV40 , that is able to transform human cells into cancer cells has been shown to integrate its DNA into a particular human chromosome , which thereby becomes a ' malignant ...
... shown us how complicated this question can be . One virus , SV40 , that is able to transform human cells into cancer cells has been shown to integrate its DNA into a particular human chromosome , which thereby becomes a ' malignant ...
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