Paperback. Zustand: Fair. No Jacket. Readable copy. Pages may have considerable notes/highlighting. ~ ThriftBooks: Read More, Spend Less.
Zustand: Good. 2nd Printing. Pages intact with minimal writing/highlighting. The binding may be loose and creased. Dust jackets/supplements are not included. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good.
Zustand: Good. 2nd Printing. Pages intact with minimal writing/highlighting. The binding may be loose and creased. Dust jackets/supplements are not included. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 24,73
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Anbieter: Revaluation Books, Exeter, Vereinigtes Königreich
EUR 37,58
Anzahl: 1 verfügbar
In den WarenkorbPaperback. Zustand: Brand New. illustrated edition. 175 pages. 10.50x8.25x0.50 inches. In Stock.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 58,76
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Verlag: Wah Yan College, Hong Kong, 2009
ISBN 10: 9628538128 ISBN 13: 9789628538126
Anbieter: Leaf and Stone Books, Toronto, ON, Kanada
Erstausgabe Signiert
Hardcover. Zustand: Good. Zustand des Schutzumschlags: No Dust Jacket. First Edition; First Printing. 250 pp. Heavily illustrated, mostly in black and white but with some color. In English with some Chinese. Gift inscription from the author on the title page. Laminated glossy hard paper covers in grey, black and white with red are clean and unmarked. Interior clean and nice, with author's inscription, otherwise unmarked. Lovely copy of this over-sized heavy book. ; 12.50 X 10.10 X 0.80 inches; 250 pages; Signed by Author.
Anbieter: Buchpark, Trebbin, Deutschland
Zustand: Sehr gut. Zustand: Sehr gut | Seiten: 56 | Sprache: Englisch | Produktart: Bücher | The hereditary retinopathy, retinitis pigmentosa (RP), which affects 1 in 3,500 people worldwide, is the most common cause of registered visual handicap among those of the working age in developed countries. RP is a highly variable disorder where patients may develop symptomatic visual loss in early childhood, while others may remain asymptomatic until mid-adulthood. Most cases of RP segregate in autosomal dominant, recessive or X-linked recessive modes, with approximately 41 genes being implicated in disease pathology to date (RetNet). The extensive genetic heterogeneity associated with autosomal dominant RP (adRP) is an undisputed hindrance to the development of genetically based therapeutics.