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 151
... common disease in this discussion of clinical biochemical genetics . I used only one example to illustrate how the principles of biochemical genetics learned from the uncommon can illuminate the common ; it is not unreasonable to ...
... common disease in this discussion of clinical biochemical genetics . I used only one example to illustrate how the principles of biochemical genetics learned from the uncommon can illuminate the common ; it is not unreasonable to ...
Seite 349
... common form of XP in which there are only skin symptoms , and a neurological form in which there can be a wide range of additional neurological abnormalities . The extreme of the neurological form , the De Sanctis - Cacchione syndrome ...
... common form of XP in which there are only skin symptoms , and a neurological form in which there can be a wide range of additional neurological abnormalities . The extreme of the neurological form , the De Sanctis - Cacchione syndrome ...
Seite 363
... common aberrations seen in different myeloproliferative disorders may be induced by a common agent . However , when one considers chronic myeloid leukaemia , where about 95 % of cases have the Philadelphia chromosome , this hypothesis ...
... common aberrations seen in different myeloproliferative disorders may be induced by a common agent . However , when one considers chronic myeloid leukaemia , where about 95 % of cases have the Philadelphia chromosome , this hypothesis ...
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