Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
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Seite 52
... Human Genetics , systematic data on the origin of human chromosome abnormalities will be available from this source . Such information must help us to solve many of the unanswered problems concerning the origin of human chromosome ...
... Human Genetics , systematic data on the origin of human chromosome abnormalities will be available from this source . Such information must help us to solve many of the unanswered problems concerning the origin of human chromosome ...
Seite 281
Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976 Salvador Armendares Sagrera. DONOR Human Cells HPRT + Θ Transformed Mouse Cells Express Human HPRT } HAT Selection 1000 RECIPIENT Mouse ...
Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976 Salvador Armendares Sagrera. DONOR Human Cells HPRT + Θ Transformed Mouse Cells Express Human HPRT } HAT Selection 1000 RECIPIENT Mouse ...
Seite 377
... human liver microsomal activity would require the use of many human liver specimens for testing a difficult experimental design . -- Another approach is the administration of foreign substances to experimental animals which are expected ...
... human liver microsomal activity would require the use of many human liver specimens for testing a difficult experimental design . -- Another approach is the administration of foreign substances to experimental animals which are expected ...
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