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 51
... Down's syndrome and parents Case Chromosomes 21 no . Conditional probability of observation for each mechanism * Father Mother Down's syndrome I ♂ II I 9 II 9 1 AB CD ABC ABD 1 ACD BCD 0 AAC AAD 0 010 100 0 0 0 BBC BBD ACC BCC 0 0 0 1 ...
... Down's syndrome and parents Case Chromosomes 21 no . Conditional probability of observation for each mechanism * Father Mother Down's syndrome I ♂ II I 9 II 9 1 AB CD ABC ABD 1 ACD BCD 0 AAC AAD 0 010 100 0 0 0 BBC BBD ACC BCC 0 0 0 1 ...
Seite 170
... Down's syndrome . A detailed cost - benefit analysis of antenatal screening for Down's syndrome in the West of Scotland has been carried out by Hagard and Carter ( 1976 ) . Their results , however , probably underestimate the value of ...
... Down's syndrome . A detailed cost - benefit analysis of antenatal screening for Down's syndrome in the West of Scotland has been carried out by Hagard and Carter ( 1976 ) . Their results , however , probably underestimate the value of ...
Seite 188
... Down's syndrome : in 1 case , a normal female was detected at amniocentesis and a male with Down's syndrome was born , while in the other a male was detected and a female with Down's syndrome was born . Discussion Frequency of and ...
... Down's syndrome : in 1 case , a normal female was detected at amniocentesis and a male with Down's syndrome was born , while in the other a male was detected and a female with Down's syndrome was born . Discussion Frequency of and ...
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