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 34
... ACTIVITY PER GRAM 3 1 10 20 30 40 50 60 75 DAYS OF AGE Fig . 1. The specific activity of ẞ - glucuronidase during postnatal development of C57BL / 6 ( upper curve ) and C3H ( lower curve ) mice . Enzyme activity in the C57BL / 6 ...
... ACTIVITY PER GRAM 3 1 10 20 30 40 50 60 75 DAYS OF AGE Fig . 1. The specific activity of ẞ - glucuronidase during postnatal development of C57BL / 6 ( upper curve ) and C3H ( lower curve ) mice . Enzyme activity in the C57BL / 6 ...
Seite 149
... activity and / or GM , gangliosidosis : clinical variants Clinical condition Tay - Sachs disease Sandhoff ... activity ' Hex A Hex B CNS disease2 1 + + 1 + 1 + + + delayed onset - = activity ( enzyme ) or disease ( CNS ) negligible or ...
... activity and / or GM , gangliosidosis : clinical variants Clinical condition Tay - Sachs disease Sandhoff ... activity ' Hex A Hex B CNS disease2 1 + + 1 + 1 + + + delayed onset - = activity ( enzyme ) or disease ( CNS ) negligible or ...
Seite 386
... activity is high during the newborn and suckling period , when milk is the prime nutrient . In the post - weaning period , lactase activity declines by about 90 % and is maintained at low levels thereafter . There are two known ...
... activity is high during the newborn and suckling period , when milk is the prime nutrient . In the post - weaning period , lactase activity declines by about 90 % and is maintained at low levels thereafter . There are two known ...
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