Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 71
... abnormal development of teeth , eyes , and kidneys ; abnormal dermato- glyphics ; persistent embryonic and fetal hemoglobin ; and abnormal enzyme levels ; all attest to the incomplete nature of development in these infants . In addition ...
... abnormal development of teeth , eyes , and kidneys ; abnormal dermato- glyphics ; persistent embryonic and fetal hemoglobin ; and abnormal enzyme levels ; all attest to the incomplete nature of development in these infants . In addition ...
Seite 132
... abnormal chromosome is delineated by its 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 ...
... abnormal chromosome is delineated by its 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 ...
Seite 321
... abnormal hemoglobins with a single amino - acid substitution in either the a or the ẞ chain have been described . One abnormal hemoglobin de- scribed recently by Jones et al . [ 1966 ] , Hb Freiburg , shows a peculiar deletion of the ...
... abnormal hemoglobins with a single amino - acid substitution in either the a or the ẞ chain have been described . One abnormal hemoglobin de- scribed recently by Jones et al . [ 1966 ] , Hb Freiburg , shows a peculiar deletion 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