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 74
... chromosomes from 76 patients with Ph ' - positive CML , who were in the acute phase , have been analyzed with banding techniques . 16 showed no change in their karyotype , whereas 60 patients had additional chromosomal abnormalities ...
... chromosomes from 76 patients with Ph ' - positive CML , who were in the acute phase , have been analyzed with banding techniques . 16 showed no change in their karyotype , whereas 60 patients had additional chromosomal abnormalities ...
Seite 75
... chromosomal abnormalities determined with banding techniques are added to my own . The data on banding patterns from the 23 patients in my series whose cells could be analyzed completely , together with the data on 37 published patients ...
... chromosomal abnormalities determined with banding techniques are added to my own . The data on banding patterns from the 23 patients in my series whose cells could be analyzed completely , together with the data on 37 published patients ...
Seite 169
... chromosomal abnormalities , and true mosaicism . To these might be added the problem of interpreting to parents chromosomal abnormalities in which the ultimate prognosis is still somewhat controversial ( XYY , XXX ) . The solution of ...
... chromosomal abnormalities , and true mosaicism . To these might be added the problem of interpreting to parents chromosomal abnormalities in which the ultimate prognosis is still somewhat controversial ( XYY , XXX ) . The solution of ...
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