Human Genetics: Proceedings of the Fifth International Congress of Human Genetics, Mexico City, 10-15 October 1976Excerpta Medica, 1977 - 408 Seiten |
Im Buch
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Seite 75
... chromosome female patients or the Y chromosome in males resulting in a chromosome number of 45. Other variants have been observed ; for example , one female patient has been reported ( Rowley , 1974 ) whose cells had 45 chromosomes ...
... chromosome female patients or the Y chromosome in males resulting in a chromosome number of 45. Other variants have been observed ; for example , one female patient has been reported ( Rowley , 1974 ) whose cells had 45 chromosomes ...
Seite 270
... chromosome constitutions and have an infinite life expectancy . Hybrids of this type invariably eliminate the human chromosomes : thus , the human chromosomes are termed the ' donor ' chromosomes , and the rodent chromosomes are ...
... chromosome constitutions and have an infinite life expectancy . Hybrids of this type invariably eliminate the human chromosomes : thus , the human chromosomes are termed the ' donor ' chromosomes , and the rodent chromosomes are ...
Seite 362
... chromosome 22 and another chromosome , usually 9 , though there are numerous instances of translocation to other chromosomes ( Lawler et al . , 1976 ) . In lymphomas there are several reports of a specific abnormality of chromosome 14 ...
... chromosome 22 and another chromosome , usually 9 , though there are numerous instances of translocation to other chromosomes ( Lawler et al . , 1976 ) . In lymphomas there are several reports of a specific abnormality of chromosome 14 ...
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