Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 197
... obtained . Analysis of their electro- phoretic mobility on a mixture of starch , agar , and polyacrylamide gel and ... obtained ( B , < B. ) . Fraction B1 migrates approximately as little as the catalase - active material obtained from ...
... obtained . Analysis of their electro- phoretic mobility on a mixture of starch , agar , and polyacrylamide gel and ... obtained ( B , < B. ) . Fraction B1 migrates approximately as little as the catalase - active material obtained from ...
Seite 467
... obtained from the census . Undoubtedly , the major problem in the use of census data for determining age- specific birth rates is the fact that much of the data on birthdates of children within a family is incomplete because of the use ...
... obtained from the census . Undoubtedly , the major problem in the use of census data for determining age- specific birth rates is the fact that much of the data on birthdates of children within a family is incomplete because of the use ...
Seite 474
... obtained using birthplaces of mates from marriage books of the last three centuries . These underestimate the immigration rates from outside the area . In the absence of a more direct estimate , for the reasons mentioned above , an ...
... obtained using birthplaces of mates from marriage books of the last three centuries . These underestimate the immigration rates from outside the area . In the absence of a more direct estimate , for the reasons mentioned above , an ...
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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Häufige Begriffe und Wortgruppen
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