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Results: 1-11 |
Results: 11
Human microphthalmia associated with mutations in the retinal homeobox gene CHX10
Authors: Percin, EF Ploder, LA Yu, JJ Arici, K Horsford, DJ Rutherford, A Bapat, B Cox, DW Duncan, AMV Kalnins, VI Kocak-Altintas, A Sowden, JC Traboulsi, E Sarfarazi, M McInnes, RR
Citation: Ef. Percin et al., Human microphthalmia associated with mutations in the retinal homeobox gene CHX10, NAT GENET, 25(4), 2000, pp. 397-401
Molecular genetics of primary congenital glaucoma
Authors: Sarfarazi, M Stoilov, I
Citation: M. Sarfarazi et I. Stoilov, Molecular genetics of primary congenital glaucoma, EYE, 14, 2000, pp. 422-428
Enhanced expression of CYP1B1 in Escherichia coli
Authors: Jansson, I Stoilov, I Sarfarazi, M Schenkman, JB
Citation: I. Jansson et al., Enhanced expression of CYP1B1 in Escherichia coli, TOXICOLOGY, 144(1-3), 2000, pp. 211-219
Papillary thyroid carcinoma associated with papillary renal neoplasia: genetic linkage analysis of a distinct heritable tumor syndrome
Authors: Malchoff, CD Sarfarazi, M Tendler, B Forouhar, F Whalen, G Joshi, V Arnold, A Malchoff, DM
Citation: Cd. Malchoff et al., Papillary thyroid carcinoma associated with papillary renal neoplasia: genetic linkage analysis of a distinct heritable tumor syndrome, J CLIN END, 85(5), 2000, pp. 1758-1764
Familial papillary thyroid carcinoma is genetically distinct from familialadenomatous polyposis coli
Authors: Malchoff, CD Sarfarazi, M Tendler, B Forouhar, F Whalen, G Malchoff, DM
Citation: Cd. Malchoff et al., Familial papillary thyroid carcinoma is genetically distinct from familialadenomatous polyposis coli, THYROID, 9(3), 1999, pp. 247-252
Visual event related potentials modulated by contextually relevant and irrelevant olfactory primes
Authors: Sarfarazi, M Cave, B Richardson, A Behan, J Sedgwick, EM
Citation: M. Sarfarazi et al., Visual event related potentials modulated by contextually relevant and irrelevant olfactory primes, CHEM SENSE, 24(2), 1999, pp. 145-154
Identification, expression and chromosome localization of a human gene encoding a novel protein with similarity to the pilB family of transcriptionalfactors (pilin) and to bacterial peptide methionine sulfoxide reductases
Authors: Huang, WH Escribano, J Sarfarazi, M Coca-Prados, M
Citation: Wh. Huang et al., Identification, expression and chromosome localization of a human gene encoding a novel protein with similarity to the pilB family of transcriptionalfactors (pilin) and to bacterial peptide methionine sulfoxide reductases, GENE, 233(1-2), 1999, pp. 233-240
Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma
Authors: Plasilova, M Stoilov, I Sarfarazi, M Kadasi, L Ferakova, E Ferak, V
Citation: M. Plasilova et al., Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma, J MED GENET, 36(4), 1999, pp. 290-294
Cause of primary congenital lymphedema - Commentary
Authors: Child, AH Beninson, J Sarfarazi, M
Citation: Ah. Child et al., Cause of primary congenital lymphedema - Commentary, ANGIOLOGY, 50(4), 1999, pp. 325-326
A gene for lymphedema-distichiasis maps to 16q24.3
Authors: Mangion, J Rahman, N Mansour, S Brice, G Rosbotham, J Child, AH Murday, VA Mortimer, PS Barfoot, R Sigurdsson, A Edkins, S Sarfarazi, M Burnand, K Evans, AL Nunan, TO Stratton, MR Jeffery, S
Citation: J. Mangion et al., A gene for lymphedema-distichiasis maps to 16q24.3, AM J HU GEN, 65(2), 1999, pp. 427-432
Mapping of primary congenital lymphedema to the 5q35.3 region
Authors: Evans, AL Brice, G Sotirova, V Mortimer, P Beninson, J Burnand, K Rosbotham, J Child, A Sarfarazi, M
Citation: Al. Evans et al., Mapping of primary congenital lymphedema to the 5q35.3 region, AM J HU GEN, 64(2), 1999, pp. 547-555
Risultati: 1-11 |