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 71
... et al . ( 1970 ) and O'Riordan et al . ( 1971 ) independently reported that the Ph ' chromosome was a No. 22 , and that it therefore should be identified as 22q- . Since Quinacrine fluorescence revealed that the chromosome present in ...
... et al . ( 1970 ) and O'Riordan et al . ( 1971 ) independently reported that the Ph ' chromosome was a No. 22 , and that it therefore should be identified as 22q- . Since Quinacrine fluorescence revealed that the chromosome present in ...
Seite 72
... et al . , 1975 ; Gahrton et al . , 1974 ; Hayata et al . , 1975 ; Mitelman , 1974 ) . In one patient , the translocation occurred between an abnormal No. 9 and a 22 ( Hayata et al . , 1975 ) . 10 cases have also been reported in which ...
... et al . , 1975 ; Gahrton et al . , 1974 ; Hayata et al . , 1975 ; Mitelman , 1974 ) . In one patient , the translocation occurred between an abnormal No. 9 and a 22 ( Hayata et al . , 1975 ) . 10 cases have also been reported in which ...
Seite 309
... et al . , 1972 , 1973 ; Jørgensen et al . , 1973 ; Mempel et al . , 1973 ; Dupont et al . , 1973 ; Van den Tweel et al . , 1973 ) . When such low responses were found the HLA - D type of the homozygote was considered present within the ...
... et al . , 1972 , 1973 ; Jørgensen et al . , 1973 ; Mempel et al . , 1973 ; Dupont et al . , 1973 ; Van den Tweel et al . , 1973 ) . When such low responses were found the HLA - D type of the homozygote was considered present within the ...
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