Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 130
... autosomal heterochromatin . Davidson and coworkers [ 5 ] have obtained evidence that at certain autosomal loci both alleles are functional in a given cell . Their experi- mental approach was to derive tissue culture cell lines from a ...
... autosomal heterochromatin . Davidson and coworkers [ 5 ] have obtained evidence that at certain autosomal loci both alleles are functional in a given cell . Their experi- mental approach was to derive tissue culture cell lines from a ...
Seite 408
... autosomal dominant . 4. Peutz - Jegher's syndrome is characterized by specific melanin pigmentation in and around the body orifices and on the digits ; there is ... autosomal dominant , but both recessive autosomal 408 CLINICAL GENETICS II.
... autosomal dominant . 4. Peutz - Jegher's syndrome is characterized by specific melanin pigmentation in and around the body orifices and on the digits ; there is ... autosomal dominant , but both recessive autosomal 408 CLINICAL GENETICS II.
Seite 414
... autosomal translocation , was condensed , the expression of the autosomal coat color gene was suppressed , while in the areas of skin where the X - chromosome with the autosomal translocated fragment was extended , there was also a ...
... autosomal translocation , was condensed , the expression of the autosomal coat color gene was suppressed , while in the areas of skin where the X - chromosome with the autosomal translocated fragment was extended , there was also a ...
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