962 results on '"Higgs, D"'
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202. Charles X of France: His Life and Times by Vincent W. Beach, and: The House of Saulx-Tavanes, Versailles and Burgundy 1700–1830 by Robert Forster (review)
203. A novel α-globin gene arrangement in man.
204. Sequence Comparison of Human and Yeast Telomeres Identifies Structurally Distinct Subtelomeric Domains.
205. Chromosomal Stabilisation by a Subtelomeric Rearrangement Involving Two Closely Related Alu Elements.
206. The alpha-thalassemia/mental retardation syndromes.
207. Vitamin C enhancement of brood rearing by caged honeybees fed a chemically defined diet.
208. α Thalassaemia in two Spanish families.
209. The interaction of alpha thalassaemia and sickle cell-beta° thalassaemia.
210. Characterization of two deletions that remove the entire human ζ-α globin gene complex (-THAI and -FIL).
211. Characterization of a new α° thalassaemia defect in the South African population.
212. 1990 MACK FORSTER PRIZE LECTURE REVIEW: The Molecular Genetics of the a globin gene family.
213. Helix pomatia agglutinin binding is a useful prognostic indicator in colorectal carcinoma.
214. Knowledge and beliefs about cancer in a socioeconomically disadvantaged population.
215. Haemoglobin gene frequencies in the Jamaican population: a study in 100,000 newborns.
216. Alpha thalassaemia in an Italian population.
217. A genetic marker for elevated levels of haemoglobin F in homozygous sickle cell disease?
218. Interaction of the ααα globin gene haplotype and sickle haemoglobin.
219. Effect of alpha thalassaemia on the rheology of homozygous sickle cell disease.
220. Thalassaemia intermedia in Cyprus: the interaction of α and β thalassaemia.
221. THE SIGNIFICANCE OF HAEMOGLOBIN H IN PATIENTS WITH MENTAL RETARDATION OR MYELOPROLIFERATIVE DISEASE.
222. Haemoglobin Constant Spring has an unstable α chain messenger RNA.
223. α-Globin gene deletions associated with Hb J Tongariki.
224. A NEW TRIPLICATED α-GLOBIN GENE ARRANGEMENT IN MAN.
225. The Genetics and Molecular Basis of Alpha Thalassaemia in Association with Hb S in Jamaican Negroes.
226. THE MOLECULAR BASIS FOR THE HAEMOGLOBIN BART'S HYDROPS FETALIS SYNDROME IN CYPRUS.
227. The Genetic Basis of Hb Q-H Disease.
228. Detection of Alpha Thalassaemia in Negro Infants.
229. Determination of Alpha Thalassaemia Phenotypes by Messenger RNA Analysis.
230. High resolution gene mapping of the human alpha globin locus.
231. G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb C.
232. Genetic and Molecular Analysis of Mild Forms of Homozygous β-Thalassemia.
233. Molecular Rearrangements of the Human α-Globin Gene Cluster.
234. THE CLINICAL AND MOLECULAR HETEROGENEITY OF THE THALASSEMIA SYNDROMES *.
235. Alpha-thalassaemia in Nigeria: Its interaction with sickle-cell disease.
236. Abnormal differentiation of leukemic cells in vitro.
237. THE DRYING OF TIMOTHY SEED 2. The rate of drying.
238. THE DRYING OF TIMOTHY SEED 1. Effect on quality.
239. THE DRYING OF TIMOTHY SEED.
240. THE DRYING OF TIMOTHY SEED.
241. The spectrophotometric determination of boron in molybdenum alloys with carmine.
242. The polarographic determination of chromium in molybdenum-chromium alloys.
243. The analysis of phosphating preparations used for the protection of steel surfaces.
244. The analysis of binary molybdenum-base alloys.
245. The estimation of boron in boronised metals.
246. Spot-tests for the identification of alloying elements in copper-base alloys.
247. Spot-tests for the detection of alloying elements in tin-base alloys.
248. Spot-tests for the detection of alloying elements in zinc-base alloys.
249. Spot-tests for the detection of alloying elements in lead-base alloys.
250. Spot-tests for the detection of alloying elements in aluminium- and magnesium-base alloys.
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