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  • Articles: DFG German National Licenses  (4)
  • 1965-1969  (4)
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  • Articles: DFG German National Licenses  (4)
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  • 1
    Electronic Resource
    Electronic Resource
    Defekt von Femur und Fibula mit Amelie, Peromelie oder ulnaren Strahldefekten der Arme Ein Syndrom (1967)
    Springer
    Human genetics 〈Berlin〉 3 (1967), S. 244-263 
    Details
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Six cases are described in which defects of the femora are associated with deformities of the upper limbs. From the available literature all cases (55) were selected in which femoral defects were associated with upper limb deformities. It became apparent that most if not all of these cases belong to a well defined syndrome. Arm deformities associated with femoral defect do not usually include the most common types, but specific rare types, namely amelia, peromelia ending at the level of the elbow, brachioradial synostosis and ulnar defects. In the syndrome in question sometimes either arm shows a different type of these deformities, which is further evidence that all cases may be considered to represent one category. In the majority of cases there is also a defect of the fibula and the fibular rays. The etiology is unknown. Familial occurrence has not been observed. Parental age does not appear to be a factor. In no case was there a thalidomide history. A history of radiation exposure during pregnancy was present in two previously published cases. Other limb deformities associated with radiation exposure in utero are quoted from the literature. Some of them are similar, but not exactly identical to the syndrome in question. Thalidomide deformities, in which the radial and tibial rays are preferentially affected, are clearly distinct. Similar defects of the femorae and fibulae but not of the arms are occasionally seen in children born to diabetic mothers.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00273126
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Zur häufigkeit und Mutationsrate des Apert-Syndroms (1967)
    Springer
    Human genetics 〈Berlin〉 4 (1967), S. 104-111 
    Details
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Description / Table of Contents: Zusammenfassung An Hand von fünf eigenen Beobachtungen wird über die Häufigkeit, die Mutationsrate und die Altersabhängigkeit des Apert-Syndroms im Regierungsbezirk Münster berichtet. Die Häufigkeit beträgt 1 auf 100000 Geburten. Die Mutationsrate liegt bei 0,4×10-5 Allele. Das durchschnittliche Alter der Väter zur Zeit der Geburt der Patienten ist mit 35 Jahren erhöht. Unsere Befunde stimmen mit den Ergebnissen von Blank in England weitgehend überein.
    Notes: Abstract Five cases of Apert's syndrome were ascertained through a systematic search of the documents of all hospitals in the governmental district Münster from 1950 to 1961. The incidence is estimated as 1 in 100000 births. Autosomal dominant heredity is assumed. The mutation rate is estimated as 0.4 · 10-5. Paternal age was 4 years in excess of that for the population. These findings are in agreement with those previously reported from England by Blank.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00291254
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Totale Syndaktylie und totale radioulnare Synostose bei zwei Brüdern (1967)
    Springer
    European journal of pediatrics 101 (1967), S. 181-190 
    Details
    ISSN: 1432-1076
    Keywords: Syndaktylie ; Mißildung der Gliedmaßen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Eine totale Syndaktylie (Löffelhand) mit radioulnarer Synostose und ungewöhnlichen Papillarmustern der Handfläche bei zwei Brüdern wird beschrieben.
    Notes: Summary Total syndactyly and radio-ulnar synostosis with unusual dermatoglyphic pattern of the plasms is described in two brothers.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00438491
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    Paper (German National Licenses)
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  • 4
    Electronic Resource
    Electronic Resource
    Darstellung, optische, magnetische Eigenschaften und Struktur von Tetrakis-n-butylammonium-hexaisothio-cyanatotitanat (III) (1969)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 365 (1969), S. 55-62 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: By reaction of anhydrous TiCl3, KSCN, and tetrabutylammonium thiocyanate in acetonitrile, crystalline [(n-C4H9)4N]3[Ti(NCS)6] has been prepared.Diffuse reflectance and solution spectra in acetonitrile and also results on the paramagnetic susceptibility from 78 to 308°K are reported. From the μeff data (evaluated according to FIGGIS' method) the spin-orbit coupling constant, the STEVENS electron delocalization parameter and the value of the axial-symmetrical field component are derived. The ligand field has trigonal symmetry. According to X-ray investigations, the space group is Th6-Pa3 and the crystallographic point symmetry of the Ti3+ ions C3 or C3i.
    Notes: Durch Umsetzung von wasserfreiem TiCl3 mit KSCN in Acetonitril bei Gegenwart von Tetrabutylammoniumrhodanid erhält man [(n-;C4H9)4N]3[Ti(NCS)6]. Reflexionsspektrum, Lösungsspektrum in Acetonitril sowie die Resultate von Messungen der paramagnetischen Suszeptibilität von 78-308°K werden mitgeteilt.Aus den nach der FIGGISschen Methode ausgewerteten μeff-Werten für verschiedene Temperaturen werden die Spin-Bahn-Kopplungskonstante, der STEVENSsche Elektronendelokalisierungsparameter sowie die Größe der axialsymmetrischen Feldkomponente abgeleitet. Das Ligandenfeld besitzt trigonale Symmetrie. Röntgenographische Untersuchungen ergeben die Raumgruppe Th6-Pa3, die Ti3+-Ionen besitzen die kristallographische Punktsymmetrie C3 bzw. C31.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19693650108
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    Paper (German National Licenses)
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