Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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Seite 274
... individuals inbred . ) The machine run is done by selecting so - called “ patriarchal ” individuals and trac- ing their relationship to the remote ancestors . These are , by and large , the parents or grandparents of the currently ...
... individuals inbred . ) The machine run is done by selecting so - called “ patriarchal ” individuals and trac- ing their relationship to the remote ancestors . These are , by and large , the parents or grandparents of the currently ...
Seite 285
... individuals who married after 1944 ; colony B 01 terminated in 1920 and D 01 in 1919 . ( 2 ) L - leut : All four clones were composed of individuals who married after 1944. The termination dates were 1918 for A 01 and B 01 , 1920 for C ...
... individuals who married after 1944 ; colony B 01 terminated in 1920 and D 01 in 1919 . ( 2 ) L - leut : All four clones were composed of individuals who married after 1944. The termination dates were 1918 for A 01 and B 01 , 1920 for C ...
Seite 428
... individuals , probably result from ovarian dysgenesis caused by the wrong dosage of the X - chromosome in the early zygote and from the variation in the timing of inactivation from tissue to tissue rather than directly from X ...
... individuals , probably result from ovarian dysgenesis caused by the wrong dosage of the X - chromosome in the early zygote and from the variation in the timing of inactivation from tissue to tissue rather than directly from X ...
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