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 15
... observations have no statistical power to test one hypothesis as compared to another . There are , for example , no statistically powerful tests that will distinguish between selective and ' neutralist ' theories of observed genic ...
... observations have no statistical power to test one hypothesis as compared to another . There are , for example , no statistically powerful tests that will distinguish between selective and ' neutralist ' theories of observed genic ...
Seite 110
... observed with deletions of various lengths . Two exceptional observations on r ( 4 ) chromosome allow a regional ... observed with a large deletion of 4p , is in fact restricted to deletion of a small segment ( Fraisse et al . , 1976 ...
... observed with deletions of various lengths . Two exceptional observations on r ( 4 ) chromosome allow a regional ... observed with a large deletion of 4p , is in fact restricted to deletion of a small segment ( Fraisse et al . , 1976 ...
Seite 288
... observed when 1s and 2s rat hepatoma cells are crossed with pseudodiploid mouse lymphoma cells . For hybrids derived from the 1s cross , extinction ( partial or complete ) is observed for all of the liver functions ; hybrids from the 2s ...
... observed when 1s and 2s rat hepatoma cells are crossed with pseudodiploid mouse lymphoma cells . For hybrids derived from the 1s cross , extinction ( partial or complete ) is observed for all of the liver functions ; hybrids from the 2s ...
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