AAAAAA

   
Results: 1-12 |
Results: 12
Clinical spectrum of fibroblast growth factor receptor mutations (vol 14, pg 115, 1999)
Authors: Passos-Bueno, MR Wilcox, WR Jabs, EW Sertie, AL Alonso, LG Kitoh, H
Citation: Mr. Passos-bueno et al., Clinical spectrum of fibroblast growth factor receptor mutations (vol 14, pg 115, 1999), HUM MUTAT, 17(5), 2001, pp. 431-431
Clinical and cytogenetic characterisation of a patient with Down syndrome resulting from a 21q22.1 -> qter duplication
Authors: Nadal, M Vigo, CG Melaragno, MI Andrade, JAD Alonso, LG Brunini, D Pritchard, M Estivill, X
Citation: M. Nadal et al., Clinical and cytogenetic characterisation of a patient with Down syndrome resulting from a 21q22.1 -> qter duplication, J MED GENET, 38(1), 2001, pp. 73-76
Average block error probability in the reverse link of a packet DS/CDMA system under Rayleigh fading channel conditions
Authors: Perez-Romero, J Alonso, LG Agusti, R
Citation: J. Perez-romero et al., Average block error probability in the reverse link of a packet DS/CDMA system under Rayleigh fading channel conditions, IEEE COMM L, 4(4), 2000, pp. 116-118
High mutation detection rate in TCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changes
Authors: Splendore, A Silva, EO Alonso, LG Richieri-Costa, A Alonso, N Rosa, A Carakushanky, G Cavalcanti, DP Brunoni, D Passos-Bueno, MR
Citation: A. Splendore et al., High mutation detection rate in TCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changes, HUM MUTAT, 16(4), 2000, pp. 315-322
Folding of a dimeric beta-barrel: Residual structure in the urea denaturedstate of the human papillomavirus E2 DNA binding domain
Authors: Mok, YK Alonso, LG Lima, LMTR Bycroft, M De Prat-Gay, G
Citation: Yk. Mok et al., Folding of a dimeric beta-barrel: Residual structure in the urea denaturedstate of the human papillomavirus E2 DNA binding domain, PROTEIN SCI, 9(4), 2000, pp. 799-811
Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia
Authors: Iughetti, P Alonso, LG Wilcox, W Alonso, N Passos-Bueno, MR
Citation: P. Iughetti et al., Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia, AM J MED G, 95(5), 2000, pp. 482-491
Neutrophil antigen 5b is carried by a protein, migrating from 70 to 95 kDa, and may be involved in neonatal alloimmune neutropenia
Authors: de Haas, M Muniz-Diaz, E Alonso, LG van der Kolk, K Kos, M Buddelmeijer, L Porcelijn, L von dem Borne, AEGK
Citation: M. De Haas et al., Neutrophil antigen 5b is carried by a protein, migrating from 70 to 95 kDa, and may be involved in neonatal alloimmune neutropenia, TRANSFUSION, 40(2), 2000, pp. 222-227
Distinctive cognate sequence discrimination, bound DNA conformation, and binding modes in the E2 C-terminal domains from prototype human and bovine papillomaviruses
Authors: Ferreiro, DU Lima, LMTR Nadra, AD Alonso, LG Goldbaum, FA de Prat-Gay, G
Citation: Du. Ferreiro et al., Distinctive cognate sequence discrimination, bound DNA conformation, and binding modes in the E2 C-terminal domains from prototype human and bovine papillomaviruses, BIOCHEM, 39(47), 2000, pp. 14692-14701
CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome
Authors: Marcelino, J Carpten, JD Suwairi, WM Gutierrez, OM Schwartz, S Robbins, C Sood, R Makalowska, I Baxevanis, A Johnstone, B Laxer, RM Zemel, L Kim, CA Herd, JK Ihle, J Williams, C Johnson, M Raman, V Alonso, LG Brunoni, D Gerstein, A Papadopoulos, N Bahabri, SA Trent, JM Warman, ML
Citation: J. Marcelino et al., CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome, NAT GENET, 23(3), 1999, pp. 319-322
Clinical spectrum of fibroblast growth factor receptor mutations
Authors: Passos-Bueno, MR Wilcox, WR Jabs, EW Sertie, AL Alonso, LG Kitoh, H
Citation: Mr. Passos-bueno et al., Clinical spectrum of fibroblast growth factor receptor mutations, HUM MUTAT, 14(2), 1999, pp. 115-125
Acute myeloid leukemia M2 and t(8;21)(q22;q22) with an unusual phenotype: myeloperoxidase (+), CD13(-), CD14(-), and CD33(-)
Authors: Vela, JAG Martin, M Delgado, I Alonso, LG Monteserin, MC Benito, L Somolinos, N Ona, F
Citation: Jag. Vela et al., Acute myeloid leukemia M2 and t(8;21)(q22;q22) with an unusual phenotype: myeloperoxidase (+), CD13(-), CD14(-), and CD33(-), ANN HEMATOL, 78(5), 1999, pp. 237-240
CD79b expression in B cell chronic lymphocytic leukemia: its implication for minimal residual disease detection
Authors: Vela, JAG Delgado, I Benito, L Monteserin, MC Alonso, LG Somolinos, N Andreau, MA Ona, F
Citation: Jag. Vela et al., CD79b expression in B cell chronic lymphocytic leukemia: its implication for minimal residual disease detection, LEUKEMIA, 13(10), 1999, pp. 1501-1505
Risultati: 1-12 |