Roach steve editors (2 risultati)
The Collector's Handbook: Tax Planning, Strategy and Estate Advice for Collectors and Their Heirs
Halperin, James L. and Rohan, Gregory J. (authors); Fleisher, Noah; Keagy, Brian; Lansdale, Steve; Meuwly, Meredith; Roach, Steve (editors)
- Brossura
Da: Books to Give ~ Books to Love®, Alexandria, VA, U.S.A.Books to Give ~ Books to Love®
Contatta il venditoreVenditore con 5 stelleCondizione: Usato - Come nuovo
EUR 17,78
Spedizione gratuitaSpedito in U.S.A.Quantità: 1 disponibili
Paperback. Condizione: As new. 11th edition. As-new copy of the eleventh editionappears to have been unread. No flaws, inside or out. Geared toward the financial and investment aspects of collecting, such as documentation, tax considerations, evaluation, charitable gifts etc.
Editore: Cambridge University Press (2004), Cambridge, 2004
- Rilegato
Da: Expatriate Bookshop of Denmark/John Jackson Books, Svendborg, DanimarcaExpatriate Bookshop of Denmark/John Jackson Books
Contatta il venditoreVenditore con 5 stelleCondizione: Usato
EUR 146,65
EUR 59,00 spedizioneSpedito da Danimarca a U.S.A.Quantità: 1 disponibili
Aggiungi al carrelloorig.boards Some light rubbing to cover corner. VG. Textual illustrations. 29x21cm, xvii,338 pp Contents: Genetics of neurocutaneous disorders; Syndrome/clinical recognition; Neurofibromatosis type 1; Neurofibromatosis type 2 D.; Tuberous sclerosis complex; Von Hippel-Lindau disease; Neurocutaneous melanosis; Basal Cell Nevus sy…ndrome; Epidermal Nevus syndrome; Multiple endocrine neoplasia type 2; Ataxia-telangiectasia; Incontinentia pigmenti; Hypomelanosis of Ito; Cowden disease; Pseudoxanthoma elasticum; Ehlers- Danlos syndrome; Progeria; Blue Rubber Bleb Nevus syndrome; Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu); Hereditary neurocutanous angiomatosis; Cutaneous hemangiomas: vascular anomaly complex; Sturge- Weber syndrome ; Lesch-Nyhan syndrome; Multiple carboxylase deficiency; Homocystinuria due to cystathionine-synthase (CBS) deficiency; Fucosidosis;Menkes Kinky Hair syndrome/Menkes disease; Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy; Cerebrotendinous xanthomatosis; Adrenoleukodystrophy; Peroximal disorders; Familial dysautonomia; Fabry disease; Giant axonal neuropathy; Chediak-Higashi syndrome; Encephalocraniocutaneous lipomatosis; Cerebello-Trigemino-Dermal dysplasia;Coffin-Siris syndrome; Lipoid proteinosis; Macrodactyl-nerve fibrolipoma. Some light rubbing to cover corner. VG.
