refsum sigvald (5 risultati)

Broschiert. Condizione: 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.

Paperback. Condizione: Very Good. Owner name on cover. Signed and inscribed to owner on first page. No text marks. Nice clean covers with light edge wear. A nice clean copy of this valuable title in rare author signed format.

Condizione: Very Good. *Price HAS BEEN REDUCED by 10% until Monday, May 18 (weekend SALE item)* 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.

pp. 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.

Condizione: 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.