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 239
... analysis is simplified . On the other hand the family environment , which is equally determined by fathers and ... analysis deals not with family resemblance but with more general relations between causes and effects . Since there may be ...
... analysis is simplified . On the other hand the family environment , which is equally determined by fathers and ... analysis deals not with family resemblance but with more general relations between causes and effects . Since there may be ...
Seite 242
... analysis is most powerful when used in conjunction with other methods to resolve heterogeneity ( Smith , 1976 ) . This is illustrated by reanalysis of the classic Colchester survey of mental retardation ( Penrose , 1938 ) ...
... analysis is most powerful when used in conjunction with other methods to resolve heterogeneity ( Smith , 1976 ) . This is illustrated by reanalysis of the classic Colchester survey of mental retardation ( Penrose , 1938 ) ...
Seite 245
... analysis using cluster analysis , 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 ...
... analysis using cluster analysis , 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 ...
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