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 13
... phenotype , population geneticists have built an elaborate , even baroque , structure of prediction of the genetic and phenotypic composition of populations . Given a particular form of genetic determination , given the mutation rates ...
... phenotype , population geneticists have built an elaborate , even baroque , structure of prediction of the genetic and phenotypic composition of populations . Given a particular form of genetic determination , given the mutation rates ...
Seite 115
... phenotype correlations , useful data can be obtained only from those cases in which only one cell line has been ... phenotype in Xp patients ; ( 2 ) the question whether or not isochromosomes of the short arm of the X chromosome exist ...
... phenotype correlations , useful data can be obtained only from those cases in which only one cell line has been ... phenotype in Xp patients ; ( 2 ) the question whether or not isochromosomes of the short arm of the X chromosome exist ...
Seite 128
... phenotypes difficult , a rough outline of a common phenotype may be sketched : horizontal palpebral clefts ( 8/8 ) , sometimes asymmetrical , enophthalmos ( 3/8 ) , micro- phthalmia ( 1/8 ) , anophthalmia ( 1/8 ) , aplasia of the nasal ...
... phenotypes difficult , a rough outline of a common phenotype may be sketched : horizontal palpebral clefts ( 8/8 ) , sometimes asymmetrical , enophthalmos ( 3/8 ) , micro- phthalmia ( 1/8 ) , anophthalmia ( 1/8 ) , aplasia of the nasal ...
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