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 47
... additional chromosome . However , with the exception of the sex chromosome abnormalities in the newborn , the precise identification of the additional chromosome had to await the advent of banding . Carr ( 1976 ) recently summarized ...
... additional chromosome . However , with the exception of the sex chromosome abnormalities in the newborn , the precise identification of the additional chromosome had to await the advent of banding . Carr ( 1976 ) recently summarized ...
Seite 74
... additional C group chromosome . The use of banding reveals that , although different additional C group chromosomes are present , one pair , a No. 8 , is involved much more frequently than the remainder . Of 37 patients whose cells ...
... additional C group chromosome . The use of banding reveals that , although different additional C group chromosomes are present , one pair , a No. 8 , is involved much more frequently than the remainder . Of 37 patients whose cells ...
Seite 78
... Additional material at the end of 14q has been reported in patients with multiple myeloma , plasma cell leukemia , Hodgkin's disease , and lymphosarcoma . In some cases , only a small additional band similar to that seen in Burkitt's ...
... Additional material at the end of 14q has been reported in patients with multiple myeloma , plasma cell leukemia , Hodgkin's disease , and lymphosarcoma . In some cases , only a small additional band similar to that seen in Burkitt's ...
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