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 194
... PRENATAL DIAGNOSIS OF GENETIC DISEASE : PRESENT SCOPE AND FUTURE POSSIBILITIES * H. GALJAARD , A. HOOGEVEEN , E. VAN DER VEER AND W.J. KLEYER Department of Cell Biology and Genetics , Medical Faculty , Erasmus University , Rotterdam ...
... PRENATAL DIAGNOSIS OF GENETIC DISEASE : PRESENT SCOPE AND FUTURE POSSIBILITIES * H. GALJAARD , A. HOOGEVEEN , E. VAN DER VEER AND W.J. KLEYER Department of Cell Biology and Genetics , Medical Faculty , Erasmus University , Rotterdam ...
Seite 195
... Prenatal sex determinations Open neural tube defects Genetic metabolic diseases tested foetuses 4206 280 2708 ** 101 ( 2.4 ... prenatal diagnosis of metabolic disorders . Unfortunately , the results Microtechniques in prenatal diagnosis 195.
... Prenatal sex determinations Open neural tube defects Genetic metabolic diseases tested foetuses 4206 280 2708 ** 101 ( 2.4 ... prenatal diagnosis of metabolic disorders . Unfortunately , the results Microtechniques in prenatal diagnosis 195.
Seite 200
... prenatal analyses for 17 different metabolic diseases ( Niermeyer et al . , 1976 ) , the microtechniques described have enabled us to establish prenatal diagnoses of glycogenosis II ( Galjaard et al . , 1973 ) , Fabry's disease ...
... prenatal analyses for 17 different metabolic diseases ( Niermeyer et al . , 1976 ) , the microtechniques described have enabled us to establish prenatal diagnoses of glycogenosis II ( Galjaard et al . , 1973 ) , Fabry's disease ...
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