Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
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... malformations usually affect the ulna and fibula . More severe malformations , such as peromelia ending at the elbow joint or total amelia of the arms , are also seen ( see Fig . 4c ) . These severe defects obviously belong to the same ...
... malformations usually affect the ulna and fibula . More severe malformations , such as peromelia ending at the elbow joint or total amelia of the arms , are also seen ( see Fig . 4c ) . These severe defects obviously belong to the same ...
Seite 105
... malformations Different congenital heart malformations References : Family Author JENNINGS & TURNER ( 1961 ) Not examined Variant present Variant present WEBER & MILLER ( 1962 ) MAKINO ( 1964 ) MOORES et al . ( 1966 ) Jennings , A. N. ...
... malformations Different congenital heart malformations References : Family Author JENNINGS & TURNER ( 1961 ) Not examined Variant present Variant present WEBER & MILLER ( 1962 ) MAKINO ( 1964 ) MOORES et al . ( 1966 ) Jennings , A. N. ...
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... malformations , i.e. , polyphenic and polyetiologic , i.e. , polygenic . We can distinguish abnormalities with ... malformations of the heart . As for TABLE 16. CEREBRO - OPHTHALMO - FACIAL MALFORMATIONS IN TRISOMY D1 Defects Number of ...
... malformations , i.e. , polyphenic and polyetiologic , i.e. , polygenic . We can distinguish abnormalities with ... malformations of the heart . As for TABLE 16. CEREBRO - OPHTHALMO - FACIAL MALFORMATIONS IN TRISOMY D1 Defects Number of ...
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