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1,459 results on '"Mark Oette"'

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201. Monosodium Urate Crystal Deposition Disease

202. McCune-Albright Syndrome

203. Slow-Transit Constipation

204. Pott’s Disease (Spine)

205. Subtype of Nemaline Myopathies or NEM3

206. Hypovitaminosis E

207. Hemosiderosis, Idiopathic Pulmonary

208. Sexual Precocity

209. Hypocalcemia with Hypercalciuria, Autosomal Dominant

210. Methylenetetrahydrofolate Reductase Deficiency

211. Hereditary Breast and Ovarian Carcinoma

212. Homocystinuria due to Cystathionine Beta-Synthase Deficiency

213. Pelizaeus-Merzbacher Disease

214. Stiff Person Syndrome

215. PME Type 1

216. Papillary Duct Ectasia

217. Sodium Channel Myotonia

218. SASD

219. Hernia, Indirect Inguinal

220. Hereditary Proteinuria Syndromes

221. Secondary Lymphedema

222. Myophosphorylase Deficiency

223. Hereditary Cerebral Amyloid Angiopathies

224. Porphyria, Variegate

225. HHT1

226. SI Deficiency

227. Pneumonia, Cryptogenic Organizing

228. Mesial Temporal Lobe Epilepsy

229. Persistent Truncus Arteriosus

230. Hemopoietic Dysplasia

231. Hyper IgE Syndrome

232. Mongolism

233. Pulmonary Valve Insufficiency

234. Pyridoxine Excess

235. Propionyl CoA Carboxylase Deficiency

236. 9p Monosomy

237. PFIC Type 2

238. Hypoxic Ischemic Encephalopathy

239. Polyendocrinopathy Ectodermal Dystrophy, Autoimmune

240. Hailey-Hailey Disease

241. Slipped Capital Femoral Epiphysis

242. Microdeletion 17p13

243. Hereditary Nonautoimmune Autosomal Dominant Toxic Thyroid Hyperplasia

244. Slow Ventricular Tachycardia

245. Primary Hyperaldosteronism

246. Monosomy 9p Syndrome

247. Hyperostosis of the Entire Skeleton

248. Hyperinsulinism/Hyperammonemia Syndrome

249. Myotonia and Paramyotonia

250. Stomatitis Aphthosa

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