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 303
... associated with the disease are alleles at the same locus . There is a suggestion that B13 and BW17 are associated with different forms of psoriasis , while no doubt the reduction in the frequency of B7 may be secondary to the increase ...
... associated with the disease are alleles at the same locus . There is a suggestion that B13 and BW17 are associated with different forms of psoriasis , while no doubt the reduction in the frequency of B7 may be secondary to the increase ...
Seite 308
... associated with the initiator events and others are associated with effector stages of cellular immunity . These have been successfully exploited to analyse the genetic requirements for cell - mediated immunity and for developing ...
... associated with the initiator events and others are associated with effector stages of cellular immunity . These have been successfully exploited to analyse the genetic requirements for cell - mediated immunity and for developing ...
Seite 347
... associated with DNA repair defects . The best established example of these diseases is xeroderma pigmentosum ( XP ) , which is in most cases associated with defects in excision repair of damaged bases ( Cleaver , 1968 ; Cleaver and ...
... associated with DNA repair defects . The best established example of these diseases is xeroderma pigmentosum ( XP ) , which is in most cases associated with defects in excision repair of damaged bases ( Cleaver , 1968 ; Cleaver and ...
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