Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
Ergebnisse 1-3 von 57
Seite 65
... mechanisms for repairing damaged genetic material are defective . This was demonstrated to be the case for one of them when decreased ' unscheduled DNA synthesis ' was found in UV - treated XP cells ( Cleaver and Bootsma , 1975 ) . DNA ...
... mechanisms for repairing damaged genetic material are defective . This was demonstrated to be the case for one of them when decreased ' unscheduled DNA synthesis ' was found in UV - treated XP cells ( Cleaver and Bootsma , 1975 ) . DNA ...
Seite 67
... mechanisms appears indicated in several other rare human genetic disorders with clinical features such as sun - sensitivity , skin hyperpigmentation , growth retardation , chromosome instability , and cancer - proneness . These include ...
... mechanisms appears indicated in several other rare human genetic disorders with clinical features such as sun - sensitivity , skin hyperpigmentation , growth retardation , chromosome instability , and cancer - proneness . These include ...
Seite 284
... MECHANISMS WHICH MAINTAIN CELL DIFFERENTIATION MARY C. WEISS Centre de Génétique Moléculaire du CNRS , Gif - sur - Yvette , France One of the many applications of somatic cell hybridization has been to explore the nature of cell ...
... MECHANISMS WHICH MAINTAIN CELL DIFFERENTIATION MARY C. WEISS Centre de Génétique Moléculaire du CNRS , Gif - sur - Yvette , France One of the many applications of somatic cell hybridization has been to explore the nature of cell ...
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 | |
30 weitere Abschnitte werden nicht angezeigt.
Andere Ausgaben - Alle anzeigen
Häufige Begriffe und Wortgruppen
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