Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
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Seite 41
... disease , but whose peripheral blood enzyme picture was quite normal ( Levy , 1976 , personal communication ) . Again , while such children may be explained eventually by other mechanisms , they are candidates for examples of congenital ...
... disease , but whose peripheral blood enzyme picture was quite normal ( Levy , 1976 , personal communication ) . Again , while such children may be explained eventually by other mechanisms , they are candidates for examples of congenital ...
Seite 149
... disease Sandhoff - Jatzkewitz disease ' A , B variant ' ' Spence variant ' Juvenile Tay - Sachs disease Adult variant ( type I ) Adult variant ( type II ) Observed enzyme activity ' Hex A Hex B CNS disease2 1 + + 1 + 1 + + + delayed ...
... disease Sandhoff - Jatzkewitz disease ' A , B variant ' ' Spence variant ' Juvenile Tay - Sachs disease Adult variant ( type I ) Adult variant ( type II ) Observed enzyme activity ' Hex A Hex B CNS disease2 1 + + 1 + 1 + + + delayed ...
Seite 303
... disease associations Disease Antigen Frequency in patients Frequency in controls ( % ) ( % ) Average relative risk Ankylosing spondylitis B27 90 8 87.8 Coeliac disease B8 71 23 Α1 64 29 Juvenile diabetes B8 37 BW15 23 Multiple sclerosis ...
... disease associations Disease Antigen Frequency in patients Frequency in controls ( % ) ( % ) Average relative risk Ankylosing spondylitis B27 90 8 87.8 Coeliac disease B8 71 23 Α1 64 29 Juvenile diabetes B8 37 BW15 23 Multiple sclerosis ...
Inhalt
The legal aspects of genetic screening and counseling | 3 |
Some trends in the study of spontaneous and induced mutation in | 19 |
Temporal genes and developmental programs | 33 |
Urheberrecht | |
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aberrations Acad activity alleles Amer amniocentesis amniotic fluid amniotic fluid cells analysis antenatal antigens assay autosomal banding biochemical blood group Bodmer cancer cell hybridization chromatid chromosome abnormalities clinical clones congenital correlation culture cytogenetic deficiency detected determined differentiation disease disorders donor Down's syndrome Editors environmental enzyme errors of metabolism extinction factors fetal fetus fibroblasts frequency functions Galjaard gene genetic distance genome H-2 complex hemoglobin HLA-D Human Genetics inborn errors individuals inheritance involved karyotype lactose Lancet linkage disequilibrium loci locus lymphocytes malformations marker maternal methods microcell Milunsky mouse mutagens mutation rates Nature Lond neural tube defects newborns normal observed parents patients phenotype phenylketonuria polymorphism population genetics possible pregnancies prenatal diagnosis Press Proc protein recent risk Ruddle samples selection somatic cell specific structural studies suggested Table techniques tissue translocation tumors variants X chromosome Zinkernagel