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 34
... structural polymorphisms it has been a simple matter to show that throughout development , from fertilization to the adult , the glucuronidase present is derived from this single structural gene . The glucuronidase developmental program ...
... structural polymorphisms it has been a simple matter to show that throughout development , from fertilization to the adult , the glucuronidase present is derived from this single structural gene . The glucuronidase developmental program ...
Seite 39
... structural genes during development , and that these distant temporal genes are sending molecular signals . Almost certainly there are receiver elements for these signals near the structural gene . The quite unexpected feature of these ...
... structural genes during development , and that these distant temporal genes are sending molecular signals . Almost certainly there are receiver elements for these signals near the structural gene . The quite unexpected feature of these ...
Seite 46
... Structural abnormalities examined detected by non - banding G - banding Phenotypically normal newborn babies 619 1 1 Phenotypically abnormal newborn babies Mentally retarded children 204 1 1 500 13 14 * Total 1,323 15 16 * * 46 , XY ...
... Structural abnormalities examined detected by non - banding G - banding Phenotypically normal newborn babies 619 1 1 Phenotypically abnormal newborn babies Mentally retarded children 204 1 1 500 13 14 * Total 1,323 15 16 * * 46 , XY ...
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