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 343
... tumors but without clinical evidence of an immunodeficiency disorder ( Fraumeni et al . , 1975a ) . Similar findings in familial stomach cancer are consistent with the reported excess of this tumor among patients with immunodeficiency ...
... tumors but without clinical evidence of an immunodeficiency disorder ( Fraumeni et al . , 1975a ) . Similar findings in familial stomach cancer are consistent with the reported excess of this tumor among patients with immunodeficiency ...
Seite 369
... tumors in patients with the genetic form of tumor . Children with genetic retinoblastoma are at greatly increased risk for osteosarcoma and this risk is still further increased by irradiation ( Sagerman et al . , 1969 ; Jensen and ...
... tumors in patients with the genetic form of tumor . Children with genetic retinoblastoma are at greatly increased risk for osteosarcoma and this risk is still further increased by irradiation ( Sagerman et al . , 1969 ; Jensen and ...
Seite 370
... tumors would therefore be different single gene disorders . Of course any pathway to homozygosity should produce tumor . If 2 carrier parents produced a homozygous child , every cell in the target tissue of a 2 - mutation tumor should ...
... tumors would therefore be different single gene disorders . Of course any pathway to homozygosity should produce tumor . If 2 carrier parents produced a homozygous child , every cell in the target tissue of a 2 - mutation tumor should ...
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