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 341
... cancers of the oral cavity , esophagus , and larynx , and also affects the risk of cancer of the liver and possibly rectum . Ultraviolet ( UV ) radiation from sunlight is the major cause of skin cancer , including melanoma . Various cancers ...
... cancers of the oral cavity , esophagus , and larynx , and also affects the risk of cancer of the liver and possibly rectum . Ultraviolet ( UV ) radiation from sunlight is the major cause of skin cancer , including melanoma . Various cancers ...
Seite 343
... cancer , primarily lymphoina . Immune defects have also been revealed in families prone to lymphoproliferative tumors but without clinical evidence of an immunodeficiency disorder ( Fraumeni et al . , 1975a ) . Similar findings in ...
... cancer , primarily lymphoina . Immune defects have also been revealed in families prone to lymphoproliferative tumors but without clinical evidence of an immunodeficiency disorder ( Fraumeni et al . , 1975a ) . Similar findings in ...
Seite 345
... cancer . This view optimizes the hopes for cancer prevention that may be achieved not only by removing environmental hazards but also by protecting high - risk individuals , and perhaps in time by modifying host mechanisms . REFERENCES ...
... cancer . This view optimizes the hopes for cancer prevention that may be achieved not only by removing environmental hazards but also by protecting high - risk individuals , and perhaps in time by modifying host mechanisms . REFERENCES ...
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