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 46
... 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 , 8p + ...
... 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 , 8p + ...
Seite 52
... abnormalities , abnormalities which affect at least 10 % of all recorded conceptions in our species . It is hoped that , by the time of the next International Congress of Human Genetics , systematic data on the origin of human ...
... abnormalities , abnormalities which affect at least 10 % of all recorded conceptions in our species . It is hoped that , by the time of the next International Congress of Human Genetics , systematic data on the origin of human ...
Seite 182
... ABNORMALITIES : A REVIEW OF TWO COLLABORATIVE STUDIES JOHN L. HAMERTON Division of Genetics , Department of Pediatrics , University of Manitoba , and Health Sciences Centre , Winnipeg , Canada The use of mid - second trimester ...
... ABNORMALITIES : A REVIEW OF TWO COLLABORATIVE STUDIES JOHN L. HAMERTON Division of Genetics , Department of Pediatrics , University of Manitoba , and Health Sciences Centre , Winnipeg , Canada The use of mid - second trimester ...
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