0
Your cart

Your cart is empty

Books

Not currently available

Disease Introduction - Kocher-Debre-Semelaigne Syndrome, Brachydactyly, Foix-Alajouanine Syndrome, Ectopia, Zymotic Disease (Paperback) Loot Price: R642
Discovery Miles 6 420
Disease Introduction - Kocher-Debre-Semelaigne Syndrome, Brachydactyly, Foix-Alajouanine Syndrome, Ectopia, Zymotic Disease...

Disease Introduction - Kocher-Debre-Semelaigne Syndrome, Brachydactyly, Foix-Alajouanine Syndrome, Ectopia, Zymotic Disease (Paperback)

Source Wikipedia

 (sign in to rate)
Loot Price R642 Discovery Miles 6 420 | Repayment Terms: R60 pm x 12*

Bookmark and Share

Supplier out of stock. If you add this item to your wish list we will let you know when it becomes available.

Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 204. Chapters: Fraser syndrome, Enterococcus faecalis, Costochondritis, Volvulus, Membranoproliferative glomerulonephritis, Central cord syndrome, Progressive bulbar palsy, Eosinophilic fasciitis, Klumpke paralysis, Heavy chain disease, Diffuse myelinoclastic sclerosis, Gianotti-Crosti syndrome, Acute aortic syndrome, Hughes-Stovin syndrome, Peroxisomal disorder, Digestive disease, Bronchorrhea, Acute proliferative glomerulonephritis, Ulnar neuropathy, Meningoencephalitis, Periodic fever, aphthous stomatitis, pharyngitis and adenitis, Pyoderma gangrenosum, CHILD syndrome, Bone marrow failure, Acute tubular necrosis, Kimura disease, Exudate, Sezary's disease, Epidermolysis bullosa dystrophica, Oligohydramnios, Trisomy 22, Danon disease, Protein toxicity, Phyllodes tumor, Oligomenorrhea, Intestinal malrotation, Super AIDS, Doege-Potter syndrome, Pitt-Hopkins syndrome, Brachydactyly, Cor triatriatum, Mixed connective tissue disease, Episodic dyscontrol syndrome, Neurogenic bladder, Young Simpson syndrome, Morquio syndrome, Cleidocranial dysostosis, CFP-10, Congenital muscular dystrophy, Laryngomalacia, Plasmacytoma, Caplan's syndrome, Retropharyngeal abscess, Factor XIII deficiency, Carotid-cavernous fistula, Osteochondrodysplasia, Hay-Wells syndrome, Blackleg (disease), Macrocephaly, Abdominal epilepsy, Duodenal atresia, Sticky platelet syndrome, Intestinal parasite, Blue rubber bleb nevus syndrome, Peritoneal mesothelioma, Dysdiadochokinesia, Familial hypocalciuric hypercalcemia, Hereditary neuropathy with liability to pressure palsy, Distal muscular dystrophy, Cervicitis, Cartilage-hair hypoplasia, Paraphrenia, Lipodermatosclerosis, Renovascular hypertension, Somnolence, Breast disease, Scimitar syndrome, Simple partial seizure, XX male syndrome, HIV/AIDS in Europe, Labyrinthine fistula, Middle cerebral artery syndrome, Fibrosis, Yunis-Varon syndrome, Sulfhemoglobinemia, Maroteaux-Lamy syndrome, Inflammatory myopathy, Female genital prolapse, Eagle syndrome, Asplenia with cardiovascular anomalies, Gray baby syndrome, Lagophthalmos, Pulmonary valve stenosis, Polymorphous light eruption, Marburg multiple sclerosis, Guyon's canal syndrome, Schmorl's nodes, Chorioamnionitis, Anti-NMDA receptor encephalitis, Perforated ulcer, Seckel syndrome, Esophagitis, Situs ambiguus, Posterior cerebral artery syndrome, Rickettsiosis, Cutis laxa, Pagophagia, Harry Raymond Eastlack, Lecithin cholesterol acyltransferase deficiency, Barakat syndrome, Melorheostosis, Sialidosis, Lofgren syndrome, Ruptured spleen, Monteggia fracture, Single umbilical artery, Arteriovenous fistula, Infantile hemangioendothelioma, Permanent neonatal diabetes mellitus, Pasma, Unstable angina, Neuropathy, ataxia, and retinitis pigmentosa, Fibromatosis, Epispadias, Hallux rigidus, Cerebrotendineous xanthomatosis, Subacute bacterial endocarditis, White sponge nevus, Congestive hepatopathy, De Barsy syndrome, Polyphagia, Hypervolemia, Preauricular sinus and cyst, Medial medullary syndrome, Branchial cleft cyst, Coronary steal, Osteopoikilosis, Sinoatrial block, Idiopathic postprandial syndrome, Volkmann's contracture, Chylothorax, Biliary colic, Acute retinal necrosis, Fissured tongue, Myocardial stunning, Sneddon's syndrome, Mallet finger, Myelophthisic anemia, Ventricular aneurysm, Vesicovaginal fistula, Kohler disease, True hermaphroditism, Intestinal atresia, Orthopnea, Melkersson-Rosenthal syndrome, Pulmonary hemorrhage, Yush disease, Light chain deposition disease, Granulomatous mastitis, Leukorrhea, Cervical ectropion, Paroxysmal cold hemoglobinuria, Photodermatitis, Amelia (birth defect), Polymorphous low-grade adenocarcinoma, Platinosis, Hereditary diffuse leukoencephalopathy with spheroids, Rapunzel syndrome, Activated protein C resistance, Aortoiliac occlusive disease, Ruzicka Goerz Anton syndrome, ...

General

Imprint: Books LLC, Wiki Series
Country of origin: United States
Release date: December 2012
First published: December 2012
Authors: Source Wikipedia
Dimensions: 246 x 189 x 11mm (L x W x T)
Format: Paperback - Trade
Pages: 308
ISBN-13: 978-1-233-26365-3
Categories: Books
Promotions
LSN: 1-233-26365-X
Barcode: 9781233263653

Is the information for this product incomplete, wrong or inappropriate? Let us know about it.

Does this product have an incorrect or missing image? Send us a new image.

Is this product missing categories? Add more categories.

Review This Product

No reviews yet - be the first to create one!

Partners