Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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DIAGNOSIS IN MEDICAL GENETICS W. LENZ Institut für Humangenetik , University of Münster Münster , Germany iagnosis is an equivocal term . It some- times means the intellectual process by which the doctor derives from observational or ...
DIAGNOSIS IN MEDICAL GENETICS W. LENZ Institut für Humangenetik , University of Münster Münster , Germany iagnosis is an equivocal term . It some- times means the intellectual process by which the doctor derives from observational or ...
Seite 50
... diagnosis and treat- ment of hereditary metabolic disease . A simple calculation reveals that the next decade could yield 2,000 intelligent potential mothers who have the phenylketonuria genotype . Should they eventually marry and bear ...
... diagnosis and treat- ment of hereditary metabolic disease . A simple calculation reveals that the next decade could yield 2,000 intelligent potential mothers who have the phenylketonuria genotype . Should they eventually marry and bear ...
Seite 71
... diagnosis . A laboratory undertaking responsibility of cytogenetic studies should be prepared to provide a sex chromatin diagnosis in less than an hour after taking the buccal smear . KLINEFELTER'S SYNDROME In chromatin - positive cases ...
... diagnosis . A laboratory undertaking responsibility of cytogenetic studies should be prepared to provide a sex chromatin diagnosis in less than an hour after taking the buccal smear . KLINEFELTER'S SYNDROME In chromatin - positive cases ...
Inhalt
Welcoming Address | 3 |
Remarks of the Secretary of the Permanent Committee for the International | 11 |
Diagnosis in medical genetics | 29 |
Urheberrecht | |
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abnormal acatalasia acatalatic acid Acta activity alleles Amer amino-acid amino-acid sequence analysis aneuploidy anomalies antibodies antigenic autosomal dominant autosomal recessive biochemical birth blood blood-group catalase cent child chromosome aberrations clinical colonies congenital consanguinity Cytogenetics defect deficiency Dept determined disaccharidases disease distribution duplication effects enzyme evolution factors female gamma globulin gene frequencies hemoglobin heredity is autosomal heterochromatin heterozygotes heterozygous Hospital Human Genetics inactivation individuals inheritance intestinal karyotype L-leut lactase Lancet leukemia linkage loci locus male malformations maltase marker marriage mating Medical mental metabolism Michigan Mongolism mosaic mutation normal observed pairs parents patients pattern pedigree peptide chains Ph¹ phenotype population possible Proc protein recombination records red cells selection sex chromatin sex-linked specific structure studies substance sucrase syndrome synthesis Table techniques tion tissue traits translocation trisomy University variable variation X-chromosome York