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Citation: J. Pantel et al., Species-specific alternative splice mimicry at the growth hormone receptorlocus revealed by the lineage of retroelements during primate evolution - A novel mechanism accounting for protein diversity between and within species, J BIOL CHEM, 275(25), 2000, pp. 18664-18669
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Citation: B. Costes et al., Prenatal detection by real-time quantitative PCR and characterization of anew CFTR deletion, 3600+15kbde15.3kb (or CFTRdele19), CLIN CHEM, 46(9), 2000, pp. 1417-1420
Citation: J. Andries et al., Modified Kelvin-Helmholtz instabilities and resonant flow instabilities ina one-dimensional coronal plume model: Results for plasma beta=0, ASTROPHYS J, 531(1), 2000, pp. 561-570
Citation: At. Csik et al., Frequency dependence of resonant absorption and over-reflection of magnetosonic waves in nonuniform structures with shear mass flow, ASTRON ASTR, 358(3), 2000, pp. 1090-1096
Citation: Y. Voitenko et M. Goossens, Competition of damping mechanisms for the phase-mixed Alfven waves in the solar corona, ASTRON ASTR, 357(3), 2000, pp. 1086-1092
Citation: A. De Groof et M. Goossens, Randomly driven fast waves in coronal loops II. with coupling to Alfven waves, ASTRON ASTR, 356(2), 2000, pp. 724-734
Authors:
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Citation: Ms. Ruderman et al., Slow surface wave damping in plasmas with anisotropic viscosity and thermal conductivity, ASTRON ASTR, 354(1), 2000, pp. 261-276
Authors:
Touraine, RL
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Citation: Rl. Touraine et al., Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brain, AM J HU GEN, 66(5), 2000, pp. 1496-1503
Authors:
Rugg, EL
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Citation: El. Rugg et al., Donor splice site mutation in keratin 5 causes in-frame removal of 22 amino acids of H1 and 1A rod domains in Dowling-Meara epidermolysis bullosa simplex, EUR J HUM G, 7(3), 1999, pp. 293-300
Authors:
Menu, E
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Citation: E. Menu et al., Selection of maternal human immunodeficiency virus type 1 variants in human placenta (vol 179, pg 44, 1999), J INFEC DIS, 179(4), 1999, pp. 1053-1053
Authors:
Fanen, P
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Citation: P. Fanen et al., Structure-function analysis of a double-mutant cystic fibrosis transmembrane conductance regulator protein occurring in disorders related to cystic fibrosis, FEBS LETTER, 452(3), 1999, pp. 371-374
Authors:
Frossard, PM
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Citation: Pm. Frossard et al., Determination of the prevalence of cystic fibrosis in the United Arab Emirates by genetic carrier screening, CLIN GENET, 55(6), 1999, pp. 496-497
Authors:
Castaldo, G
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Citation: G. Castaldo et al., Detection of five rare cystic fibrosis mutations peculiar to southern Italy: Implications in screening for the disease and phenotype characterizationfor patients with homozygote mutations, CLIN CHEM, 45(7), 1999, pp. 957-962
Citation: B. Pinter et M. Goossens, Oscillations in a magnetic solar model - I. Parallel propagation in a chromospheric and coronal magnetic field with constant Alfven speed, ASTRON ASTR, 347(1), 1999, pp. 321-334
Authors:
Pennarun, G
Escudier, E
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Cacheux, V
Roger, G
Clement, A
Goossens, M
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Citation: G. Pennarun et al., Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia, AM J HU GEN, 65(6), 1999, pp. 1508-1519
Authors:
Danan, C
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Citation: C. Danan et al., Evaluation of parental mitochondrial inheritance in neonates born after intracytoplasmic sperm injection, AM J HU GEN, 65(2), 1999, pp. 463-473
Authors:
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Citation: C. Cazeneuve et al., MEFV-gene analysis in Armenian patients with familial Mediterranean fever:Diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype - Genetic and therapeutic implications, AM J HU GEN, 65(1), 1999, pp. 88-97