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 170
... least in Great Britain and the United States , approximately 1-2 % of births are to women over age 40 , 7-8 % to ... least 45 inborn errors of metabolism are potentially diagnosable in utero because the relevant enzyme has been ...
... least in Great Britain and the United States , approximately 1-2 % of births are to women over age 40 , 7-8 % to ... least 45 inborn errors of metabolism are potentially diagnosable in utero because the relevant enzyme has been ...
Seite 245
... least squares and minimum path techniques with the correct topology . Even for a small number of populations ( 6 ) and 20 characters the results were not encouraging , and with 15 populations and 20 characters the chance of obtaining ...
... least squares and minimum path techniques with the correct topology . Even for a small number of populations ( 6 ) and 20 characters the results were not encouraging , and with 15 populations and 20 characters the chance of obtaining ...
Seite 356
... least some cases but there is no clear evidence of clone formation . In some patients where leukaemias have been treated with cytotoxic drugs it is possible that some of the abnormal stem lines that emerge are not only the consequence ...
... least some cases but there is no clear evidence of clone formation . In some patients where leukaemias have been treated with cytotoxic drugs it is possible that some of the abnormal stem lines that emerge are not only the consequence ...
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