Sprache: Englisch
Verlag: Ejnar Munksgaard, 1946
Anbieter: books4less (Versandantiquariat Petra Gros GmbH & Co. KG), Welling, Deutschland
Broschiert. Zustand: Gut. 303 Seiten; Das hier angebotene Buch stammt aus einer teilaufgelösten wissenschaftlichen Bibliothek und trägt die entsprechenden Kennzeichnungen (Rückenschild, Instituts-Stempel.); der Buchzustand ist ansonsten ordentlich und dem Alter entsprechend gut. Einbandkanten sind leicht bestoßen. In ENGLISCHER Sprache. Sprache: Englisch Gewicht in Gramm: 670.
Verlag: Universitetsforlaget, 1963
Anbieter: Zubal-Books, Since 1961, Cleveland, OH, USA
Zustand: Very Good. 363 pp., softcover, very good. - If you are reading this, this item is actually (physically) in our stock and ready for shipment once ordered. We are not bookjackers. Buyer is responsible for any additional duties, taxes, or fees required by recipient's country.
Verlag: Johan Grundt Tanum. Oslo, 1946
Anbieter: Patrick Pollak Rare Books ABA ILAB, SOUTH BRENT, DEVON, Vereinigtes Königreich
EUR 142,56
Anzahl: 1 verfügbar
In den Warenkorbpp. 303, (i). 28 illustrations. Original printed wrappers a bit dusty and soft at the edges, backstrp split at the front edge, uncut, author's inscription and name stamp of MACDONALD CRITCHLEY with his notes on the wrappers verso, *GARRISON-MORTON #3924.2 'Refsum's Syndrome', an inherited disorder of lipid metabolism. TOGETHER WITH : NEVIN, N. C., CUMINGS, J. N. and MCKEOWN, F. Refsum's Syndrome. Heredopathia Atactica Polyneuritiformis. Offprint from 'BRAIN', v.90, pt.II, pp. 419-428. 1967. Original wrappers, stapled, creased at fore-edge, else a good copy.
Verlag: Munksgaard (1990), Copenhagen, 1990
Anbieter: Expatriate Bookshop of Denmark, Svendborg, Dänemark
Zustand: Minor rubbing. VG. orig.boards Minor rubbing. VG. Textual tables & diagrams 25x16cm, 313 pp Contains 20 papers. Includes: J.G. Hall "The Potential Importance of Imprinting in Explaining Common Disorders"; C.F. Sing & P.P. Moll " Strategies for Unravelling the Genetic Basis of Coronary Artery Disease"; D.J. Galton "DNA Variation of the Apolipoprotein Loci & Risk for Coronary Artherosclerosis"; K. Berg "Level Genes & Variability Genes in the Etiology of Hyperlipidemia & Artherosclerosis"; J. Scott, Et al: "RNA Editing: A Novel Mechanism for Regulating Lipid Transport from the Intestine"; J.C. Pedersen & K. Berg "Normal Genetic Polymorpohism at the LDL Receptor Locus & Lipid Levels"; J. Rapacz & J. Hasler-Rapacz "The Pig as a Model for Studying Genetic Polymorphisms of Apolipoproteins in Relation to Lipid Levels & Artherosclerosis"; K. Berg "Genetics of Atherogenic Lp(a) Lipoprotein"; G. Dahlen "Clinical Significance of Lp(a) Lipoprotein"; A.M. Scanu "Lp(a) in Non-human Primates: Relation to Man"; J.J. Mulvihill "From Phenotype to Gene in Preneoplastic Mendelian Disorders: Example of Neurofibromatosis 1 (Recklinghausen Disease)"; H. Luthman; et al: "Molecular Genetic Studies of the Etiology of Non-Insulin-Dependent Diabetes Mellitus"; W.O.C.M. Cookson "Towards a Gene for Atopy & Atopic Asthma"; J.B. Natvig; et al: "Inherited Susceptibility to Rheumatoid Arthritis"; C.R. Cloninger "Gene-Environment Interaction in the Development of Personality & Its Disorders"; J.L. Kennedy; et al: " Searching for Genes Predisposing to Neuropsychiatric Disorders"; K.S. Kendler "Schizophrenia as a Complex Phenotype"; S.B. Guze "Genetic Aspects.