Human Heredity, Volume 23Karger., 1969 - Biometry |
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Page 318
... chromosomes from a D / G translocation Down's syndrome ( case No. 3 ) . a Routine preparation . b C band . c G band . Arrow showing the translocation chromosome . translocation chromosome is less prominent in comparison to that of the F ...
... chromosomes from a D / G translocation Down's syndrome ( case No. 3 ) . a Routine preparation . b C band . c G band . Arrow showing the translocation chromosome . translocation chromosome is less prominent in comparison to that of the F ...
Page 321
22 chromosome , it is interpreted that the missing 22 chromosome is involved in the formation of the abnormal chromosome . The origin of the other arm of this chromosome is a matter of conjecture . Most probably , the 22 chromo- some ...
22 chromosome , it is interpreted that the missing 22 chromosome is involved in the formation of the abnormal chromosome . The origin of the other arm of this chromosome is a matter of conjecture . Most probably , the 22 chromo- some ...
Page 561
... chromosome . The majority of cells contained 46 chromosomes with a partially deleted number 9 chromosome and a chromosomal fragment . From these data and others repor- ted , it would appear that there is a susceptibility for breakage of ...
... chromosome . The majority of cells contained 46 chromosomes with a partially deleted number 9 chromosome and a chromosomal fragment . From these data and others repor- ted , it would appear that there is a susceptibility for breakage of ...
Contents
Pigment Spotting in Man and the Number | 1 |
Skin Melanin Content in BlueEyed | 13 |
Risk of Recurrence and Carrier | 19 |
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abnormal Acta genet Ag(x Åland Islands allele ALPER analysis antibody antigen BECKMAN birth blood group blood samples BRÖNNESTAM C3 phenotypes cell acid phosphatase cholinesterase chromosome clinical complement component correlation dermatoglyphic dibucaine distribution ear lobe effect enzyme ERIKSSON erythrocytes estimates factors females G band gallstone gel electrophoresis gene frequencies genetic markers Genetic polymorphism genotypes GIBLETT GOEDDE haemoglobin Heredity heterozygotes Human Hered Humangenetik India individuals inheritance investigation isozyme Key Words kinship Lapps linkage loci males malformations migration normal Norwegian observed obtained offspring Old Believer parents parishes patients patterns phenotypes pigmentation Population Genetics population studies propositus protein recombination red cell acid red cell enzyme reported Request reprints rheumatoid arthritis ridge count sera short arm showed sibship significant Spanish populations starch gel superoxide dismutase Sweden syndrome Table TEISBERG tested Total trait types Umeå values variants