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 179
... samples where an elevated ( more than +3 S.D. ) AFP concentration is determined . The Betke - Kleihauer test22 may not be as useful in samples sent by mail since the red blood cells may hemolyze spontaneously before examination ...
... samples where an elevated ( more than +3 S.D. ) AFP concentration is determined . The Betke - Kleihauer test22 may not be as useful in samples sent by mail since the red blood cells may hemolyze spontaneously before examination ...
Seite 217
... samples daily from the hospitals in Mexico City and delivers them to the laboratory . Samples from Zamora are sent by bus once a week and the same messenger picks them up at the bus terminal . Samples from the Tzotzil infants are sent ...
... samples daily from the hospitals in Mexico City and delivers them to the laboratory . Samples from Zamora are sent by bus once a week and the same messenger picks them up at the bus terminal . Samples from the Tzotzil infants are sent ...
Seite 221
... samples ( 2480 collected before 10 days of life , 2463 at 1 month of age ) , no cases were found of a specific ... samples . In 5.2 % the aniline phosphate spot test was positive ; additional paper chromatography revealed that 62.1 % of ...
... samples ( 2480 collected before 10 days of life , 2463 at 1 month of age ) , no cases were found of a specific ... samples . In 5.2 % the aniline phosphate spot test was positive ; additional paper chromatography revealed that 62.1 % 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