Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 116
... caused by this aberration . Truly specific effects due to a single locus are required . These symptoms may be called basic ... cause characteristic contractures in trisomy 18. In trisomy 21 , however , clinodactyly— seen also in other ...
... caused by this aberration . Truly specific effects due to a single locus are required . These symptoms may be called basic ... cause characteristic contractures in trisomy 18. In trisomy 21 , however , clinodactyly— seen also in other ...
Seite 321
... cause single amino - acid substitutions or deletions of some residues . Both these events can be observed in ... caused by an unequal crossing - over [ Jones et al . , 1966 ] . The amino - acid changes which are observed between ...
... cause single amino - acid substitutions or deletions of some residues . Both these events can be observed in ... caused by an unequal crossing - over [ Jones et al . , 1966 ] . The amino - acid changes which are observed between ...
Seite 465
... cause of a fertility difference . Thus the only causes of a reproductivity difference which can be reasonably identified by census data relate to marriage pat- terns and their stability as a function of age , and the distribution of the ...
... cause of a fertility difference . Thus the only causes of a reproductivity difference which can be reasonably identified by census data relate to marriage pat- terns and their stability as a function of age , and the distribution of 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