Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 126
... relatively short period of time , but even then continue after almost all other members of the complement have ceased . Taylor [ 28 ] and Hsu [ 17 ] have shown that certain regions which are inactive early in S become the relatively ...
... relatively short period of time , but even then continue after almost all other members of the complement have ceased . Taylor [ 28 ] and Hsu [ 17 ] have shown that certain regions which are inactive early in S become the relatively ...
Seite 132
... relatively heavy uptake of label , indicating that it was very actively engaged in DNA synthesis . This abnormal X was the late - replicating X in all cells examined . Certain autosomes in this cell ( e.g. , Nos . 4 and 16 ) are ...
... relatively heavy uptake of label , indicating that it was very actively engaged in DNA synthesis . This abnormal X was the late - replicating X in all cells examined . Certain autosomes in this cell ( e.g. , Nos . 4 and 16 ) are ...
Seite 510
... relatively older ovary that may lead to an egg in which nondisjunction takes place and it is the genetic fact of having three chromosomes 21 in the cells of the embryo which leads to its abnormal development . Within close limits the ...
... relatively older ovary that may lead to an egg in which nondisjunction takes place and it is the genetic fact of having three chromosomes 21 in the cells of the embryo which leads to its abnormal development . Within close limits the ...
Inhalt
Welcoming Address | 3 |
Remarks of the Secretary of the Permanent Committee for the International | 11 |
Diagnosis in medical genetics | 29 |
Urheberrecht | |
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abnormal acatalasia acatalatic acid Acta activity alleles Amer amino-acid amino-acid sequence analysis aneuploidy anomalies antibodies antigenic autosomal dominant autosomal recessive biochemical birth blood blood-group catalase cent child chromosome aberrations clinical colonies congenital consanguinity Cytogenetics defect deficiency Dept determined disaccharidases disease distribution duplication effects enzyme evolution factors female gamma globulin gene frequencies hemoglobin heredity is autosomal heterochromatin heterozygotes heterozygous Hospital Human Genetics inactivation individuals inheritance intestinal karyotype L-leut lactase Lancet leukemia linkage loci locus male malformations maltase marker marriage mating Medical mental metabolism Michigan Mongolism mosaic mutation normal observed pairs parents patients pattern pedigree peptide chains Ph¹ phenotype population possible Proc protein recombination records red cells selection sex chromatin sex-linked specific structure studies substance sucrase syndrome synthesis Table techniques tion tissue traits translocation trisomy University variable variation X-chromosome York