768 results on '"Clegg, J. B."'
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252. DNA INVERSION AND GENE DELETION IN Gy(Δβ)° THALASSAEMIA
253. Comparison of electrical defects in Ge+and Si+preamorphized BF2‐implanted silicon
254. Characterization of shallow (Rp<20 nm) As‐ and B‐implanted and electron‐beam annealed silicon
255. HB F-Granada or α2Gγ222 (B4)ASP→VAL: A New Human Fetal Hemoglobin Variant
256. THE CLINICAL AND CHEMICAL HETEROGENEITY OF THE ?-THALASSEMIAS
257. Haemoglobin Radcliffe (α2β299(G1)Ala): A High Oxygen‐Affinity Variant Causing Familial Polycythaemia
258. Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.
259. A MOUSE β-GLOBIN MUTANT THAT IS AN EXACT MODEL OF HEMOGLOBIN RAINIER IN MAN
260. Genetic and Molecular Analysis of Mild Forms of Homozygous ?-Thalassemia
261. α-Globin gene deletions associated with Hb J Tongariki
262. Restriction endonuclease maps of the β-like globin gene cluster in the British and Greek forms of HPFH, and for one example ofGγβ+HPFH
263. High frequency of beta thalassaemia in a small island population in Melanesia.
264. Alpha thalassaemia in British people.
265. Electrically active defects in shallow pre-amorphisedp + n junctions in silicon
266. Dynamic range of 106in depth profiling using secondary‐ion mass spectrometry
267. Haemoglobin Bart's hydrops syndrome in Greece.
268. The Structure of Hemoglobin Hopkins-2
269. Migration of Si in δ-doped GaAs
270. Haemoglobin F(Malta): a New Foetal Haemoglobin Variant with a High Incidence in Maltese Infants
271. Hereditary Persistence of Foetal Haemoglobin associated with a γβ Fusion Variant, Haemoglobin Kenya
272. Thalassaemia in the British
273. An Improved Method for the Characterization of Human Haemoglobin Mutants: Identification of α2β295GLU, Haemoglobin N (Baltimore)
274. Hemoglobin Philly (β35 tyrosine→phenylalanine): studies in the molecular pathology of hemoglobin
275. Separation of the α and β-Chains of Human Haemoglobin
276. Thalassaemia in an Irish family
277. Polycythemia associated with a hemoglobinopathy.
278. Haemoglobin Synthesis in α-Thalassaemia (Haemoglobin H Disease)
279. Reduction in secondary ion fogging on photographic plates used in mass spectrography
280. Haemoglobin Synthesis during Erythroid Maturation in β-Thalassaemia
281. Two New Haemoglobin Variants involving Proline Substitutions
282. Cold Spring Harbor Symposia on Quantitative Biology, Vol. XXXIV
283. Haemoglobin synthesis in thalassaemia
284. The N-Terminal Sequence of Bovine Carboxypeptidase A and Its Relation to Zymogen Activation*
285. Preliminary surveys for the prevalence of the thalassaemia genes in some African populations
286. C-Terminal Half of Immunoglobulin λ Chains
287. Synthesis in vitro of Anti-Lepore Haemoglobin
288. Distribution of impurities in semi‐insulating GaAs after heat treatment in hydrogen
289. Chromium and iron impurities in liquid encapsulated Czochralski gallium arsenide
290. Secondary ion mass spectrometry study of lightly doped p‐type GaAs films grown by molecular beam epitaxy
291. Comparison of electrical defects in Ge+ and Si+ preamorphized BF2-implanted silicon.
292. Characterization of shallow (Rp <20 nm) As- and B-implanted and electron-beam annealed silicon.
293. Can the product of the \[thetas] gene be a real globin?
294. Molecular genetics of mammalian haemoglobins.
295. Evidence for mitochondrial DNA recombination in a human population of island Melanesia: correction
296. Electrical Characterisation of Shallow Pre-Amorphised +n junctions in silicon.
297. Detection of the Factor V Leiden Mutation Using Whole Blood PCR
298. Carbon, oxygen and silicon impurities in gallium arsenide.
299. Summary Abstract: The effect of the oxygen concentration on the electrical and optical properties of AlGaAs films grown by MBE.
300. ChemInform Abstract: Experimental Study of Diffusion and Interface Segregation of P in an LPCVD Si-Carbon Emitter Structure.
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