Proceedings of the ... International Congress of Human Genetics, Band 3S. Karger, 1967 - 578 Seiten |
Im Buch
Ergebnisse 1-3 von 67
Seite 390
... hand likewise is a major target for sunlight exposure . Vesicular and bullous eruptions develop on the dorsum of the hands with subsequent scarring , hyperpigmentation , and occasionally basal cell carcinomatous changes . The heredity ...
... hand likewise is a major target for sunlight exposure . Vesicular and bullous eruptions develop on the dorsum of the hands with subsequent scarring , hyperpigmentation , and occasionally basal cell carcinomatous changes . The heredity ...
Seite 397
... hand is small , and syndactyly or cleft hand is seen ; the nails show considerable variation , from hypoplasia to increased thickness . The heredity is autosomal recessive . 7. Werner's syndrome refers to premature senile changes which ...
... hand is small , and syndactyly or cleft hand is seen ; the nails show considerable variation , from hypoplasia to increased thickness . The heredity is autosomal recessive . 7. Werner's syndrome refers to premature senile changes which ...
Seite 408
... hand shows pigmented spots distributed over the palmar aspect of the fingers . The heredity is autosomal dominant . X. CHRONIC RENAL Tubular Insufficiency SyndROMES 1. de Toni - Fanconi syndrome is a rare cystine storage disease ...
... hand shows pigmented spots distributed over the palmar aspect of the fingers . The heredity is autosomal dominant . X. CHRONIC RENAL Tubular Insufficiency SyndROMES 1. de Toni - Fanconi syndrome is a rare cystine storage disease ...
Inhalt
Welcoming Address | 3 |
Remarks of the Secretary of the Permanent Committee for the International | 11 |
Diagnosis in medical genetics | 29 |
Urheberrecht | |
35 weitere Abschnitte werden nicht angezeigt.
Andere Ausgaben - Alle anzeigen
Häufige Begriffe und Wortgruppen
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