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 133
... deficiency , e.g. deficiency of a - L - iduronidase 5. Different ( presumably allelic ) forms of enzyme deficiency , e.g. those present in the Hurler and Scheie syndromes . The ultimate in taxonomy is possible when the specific ...
... deficiency , e.g. deficiency of a - L - iduronidase 5. Different ( presumably allelic ) forms of enzyme deficiency , e.g. those present in the Hurler and Scheie syndromes . The ultimate in taxonomy is possible when the specific ...
Seite 211
... deficiency Propionyl - CoA carboxylase deficiency Succinyl - CoA : 3 - ketoacid Co A - transferase deficiency Vitamin B12 metabolic defect Miscellaneous disorders Acatalasemia Acute intermittent porphyria Adenosine deaminase deficiency ...
... deficiency Propionyl - CoA carboxylase deficiency Succinyl - CoA : 3 - ketoacid Co A - transferase deficiency Vitamin B12 metabolic defect Miscellaneous disorders Acatalasemia Acute intermittent porphyria Adenosine deaminase deficiency ...
Seite 382
... deficiency is widespread in the United States and more common in most underdeveloped countries ( Cook and Finch , 1975 ) . This iron deficiency leads to anemia , but even in the absence of anemia appears to interfere with physical ...
... deficiency is widespread in the United States and more common in most underdeveloped countries ( Cook and Finch , 1975 ) . This iron deficiency leads to anemia , but even in the absence of anemia appears to interfere with physical ...
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