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 72
... translocation has been identified in 242 ( see references in Rowley , 1977 , for review up to late 1975 ) . Recently , 18 cases with either unusual or complex translocations , accounting for 7.0 % of all Ph ' - positive patients , have ...
... translocation has been identified in 242 ( see references in Rowley , 1977 , for review up to late 1975 ) . Recently , 18 cases with either unusual or complex translocations , accounting for 7.0 % of all Ph ' - positive patients , have ...
Seite 78
... translocated elsewhere ( Harnden , 1977 ; McCaw et al . , 1977 ) . The translocation site may be the end of the other No. 14 , in a tandem 14q : 14q translocation . Other chromosomes in the complement may also be involved in the ...
... translocated elsewhere ( Harnden , 1977 ; McCaw et al . , 1977 ) . The translocation site may be the end of the other No. 14 , in a tandem 14q : 14q translocation . Other chromosomes in the complement may also be involved in the ...
Seite 79
... translocations , for example , the 9 ; 22 and 8 ; 21 translocations in myeloid cells and the 8 ; 14 translocation in lymphocytes , are only viable in the tissue in which they are found . The recent report of the 9 ; 22 translocation in ...
... translocations , for example , the 9 ; 22 and 8 ; 21 translocations in myeloid cells and the 8 ; 14 translocation in lymphocytes , are only viable in the tissue in which they are found . The recent report of the 9 ; 22 translocation in ...
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