-
2
-
-
0025134810
-
Gradient of distribution in Europe of the major CF mutation and of its associated haplotype
-
EWGCFG European Working Group on Cystic Fibrosis Genetics. Gradient of distribution in Europe of the major CF mutation and of its associated haplotype. Hum Genet 85 (1990) 436-445
-
(1990)
Hum Genet
, vol.85
, pp. 436-445
-
-
EWGCFG European Working Group on Cystic Fibrosis Genetics1
-
3
-
-
0027326193
-
Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers
-
Morral N., Nunes V., Casals T., Chillón M., Giménez J., Bertranpetit J., et al. Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers. Hum Mol Genet 2 (1993) 1015-1022
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1015-1022
-
-
Morral, N.1
Nunes, V.2
Casals, T.3
Chillón, M.4
Giménez, J.5
Bertranpetit, J.6
-
4
-
-
0028062781
-
Cystic fibrosis heterozygote resistance to cholera toxin in the cystic fibrosis mouse model
-
Gabriel S.E., Bringman K.N., Koller B.H., Boucher R.C., and Stutts M.J. Cystic fibrosis heterozygote resistance to cholera toxin in the cystic fibrosis mouse model. Science 266 (1994) 107-109
-
(1994)
Science
, vol.266
, pp. 107-109
-
-
Gabriel, S.E.1
Bringman, K.N.2
Koller, B.H.3
Boucher, R.C.4
Stutts, M.J.5
-
5
-
-
0029016718
-
Protection against bronchial asthma by CFTR delta F508 mutation: a heterozygote advantage in cystic fibrosis
-
Schroeder S.A., Gaughan D.M., and Swift M. Protection against bronchial asthma by CFTR delta F508 mutation: a heterozygote advantage in cystic fibrosis. Nat Med 1 (1995) 1100-1102
-
(1995)
Nat Med
, vol.1
, pp. 1100-1102
-
-
Schroeder, S.A.1
Gaughan, D.M.2
Swift, M.3
-
6
-
-
0032492855
-
Salmonella typhi uses CFTR to enter intestinal epithelial cells
-
Pier G.B., Grout M., Zaidi T., Meluleni G., Mueschenborn S., Banting G., et al. Salmonella typhi uses CFTR to enter intestinal epithelial cells. Nature 393 (1998) 79-82
-
(1998)
Nature
, vol.393
, pp. 79-82
-
-
Pier, G.B.1
Grout, M.2
Zaidi, T.3
Meluleni, G.4
Mueschenborn, S.5
Banting, G.6
-
7
-
-
0036138110
-
Can a place of origin of the main cystic fibrosis mutation be identified?
-
Mateu E., Calafell F., Ramos M.D., Casals T., and Bertranpetit J. Can a place of origin of the main cystic fibrosis mutation be identified?. Am J Hum Genet 70 (2002) 257-264
-
(2002)
Am J Hum Genet
, vol.70
, pp. 257-264
-
-
Mateu, E.1
Calafell, F.2
Ramos, M.D.3
Casals, T.4
Bertranpetit, J.5
-
8
-
-
0028877929
-
Geographic and ethnic distribution of the more frequent cystic fibrosis mutations in Europe show that a founder effect is apparent for several mutant alleles
-
Lucotte G., and Hazout S. Geographic and ethnic distribution of the more frequent cystic fibrosis mutations in Europe show that a founder effect is apparent for several mutant alleles. Hum Biol 67 (1995) 561-576
-
(1995)
Hum Biol
, vol.67
, pp. 561-576
-
-
Lucotte, G.1
Hazout, S.2
-
9
-
-
0030754623
-
Biomed CF mutation analysis consortium. Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations
-
Estivill X., Bancells C., and Ramos C. Biomed CF mutation analysis consortium. Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations. Hum Mutat 10 (1997) 135-154
-
(1997)
Hum Mutat
, vol.10
, pp. 135-154
-
-
Estivill, X.1
Bancells, C.2
Ramos, C.3
-
10
-
-
34247153134
-
Enfermedad Fibroquística del páncreas
-
Emiliani R.A. (Ed), Libreria Técnica, CP 67 SA. Buenos Aires
-
Pivetta O.H., Luna M.C., Granados P., and Cafferata E.G. Enfermedad Fibroquística del páncreas. In: Emiliani R.A. (Ed). Gastroenterología en clínica pediátrica (1997), Libreria Técnica, CP 67 SA. Buenos Aires 190-221
-
(1997)
Gastroenterología en clínica pediátrica
, pp. 190-221
-
-
Pivetta, O.H.1
Luna, M.C.2
Granados, P.3
Cafferata, E.G.4
-
11
-
-
0031048465
-
Spectrum of CFTR mutations in Argentine cystic fibrosis patients
-
Chertkoff L., Visich A., Bienvenu T., Grenoville M., Segal E., Carniglia L., et al. Spectrum of CFTR mutations in Argentine cystic fibrosis patients. Clin Genet 51 (1997) 43-47
-
(1997)
Clin Genet
, vol.51
, pp. 43-47
-
-
Chertkoff, L.1
Visich, A.2
Bienvenu, T.3
Grenoville, M.4
Segal, E.5
Carniglia, L.6
-
12
-
-
0036524147
-
Complete screening of the CFTR gene in Argentine cystic fibrosis patients
-
Visich A., Zielenski J., Castanos C., Diez G., Grenoville M., Segal E., et al. Complete screening of the CFTR gene in Argentine cystic fibrosis patients. Clin Genet 61 (2002) 207-213
-
(2002)
Clin Genet
, vol.61
, pp. 207-213
-
-
Visich, A.1
Zielenski, J.2
Castanos, C.3
Diez, G.4
Grenoville, M.5
Segal, E.6
-
13
-
-
0343527249
-
Spectrum of CFTR mutations in Mexican cystic fibrosis patients: identification of five novel mutations (W1098C, 846delT, P750L, 4160insGGGG and 297-1G→A)
-
Orozco L., Velasquez R., Zielenski J., Tsui L.C., Chávez M., Lezana J.L., et al. Spectrum of CFTR mutations in Mexican cystic fibrosis patients: identification of five novel mutations (W1098C, 846delT, P750L, 4160insGGGG and 297-1G→A). Hum Genet 106 (2000) 360-365
-
(2000)
Hum Genet
, vol.106
, pp. 360-365
-
-
Orozco, L.1
Velasquez, R.2
Zielenski, J.3
Tsui, L.C.4
Chávez, M.5
Lezana, J.L.6
-
14
-
-
34247126197
-
Main cystic fibrosis mutations in patients from Colombia: implications of the mutational spectrum for local and regional molecular diagnosis programs
-
Mutation in Brief # 644 Online
-
Keyeux G., Rodas M.C., Bienvenu T., Garavito P., Vidaud D., Sanchez D., et al. Main cystic fibrosis mutations in patients from Colombia: implications of the mutational spectrum for local and regional molecular diagnosis programs. Hum Mutat (2003) 1-7 Mutation in Brief # 644 Online
-
(2003)
Hum Mutat
, pp. 1-7
-
-
Keyeux, G.1
Rodas, M.C.2
Bienvenu, T.3
Garavito, P.4
Vidaud, D.5
Sanchez, D.6
-
15
-
-
10744221410
-
High allelic heterogeneity between Afro-Brazilians and Euro-Brazilians impacts cystic fibrosis genetic testing
-
Raskin S., Pereira L., Reis F., Rosario N.A., Ludwig N., and Valentim L. High allelic heterogeneity between Afro-Brazilians and Euro-Brazilians impacts cystic fibrosis genetic testing. Gen Test 7 (2003) 213-218
-
(2003)
Gen Test
, vol.7
, pp. 213-218
-
-
Raskin, S.1
Pereira, L.2
Reis, F.3
Rosario, N.A.4
Ludwig, N.5
Valentim, L.6
-
16
-
-
34247134067
-
-
WHO (2004) The Molecular Genetic Epidemiology of Cystic Fibrosis. Report of a Joint Meeting of WHO/ECFTN/ICF(M)A/ECFS. http://www.who.org/genomics.
-
-
-
-
17
-
-
0024994250
-
The frequency of the CF Delta F508 deletion in CF chromosomes of different ethnic origin
-
Aulehla-Scholz C., Kaiser R., Weber J., Pivetta O.H., Eigel A., Dworniczak B., et al. The frequency of the CF Delta F508 deletion in CF chromosomes of different ethnic origin. Hum Genet 85 (1990) 392-393
-
(1990)
Hum Genet
, vol.85
, pp. 392-393
-
-
Aulehla-Scholz, C.1
Kaiser, R.2
Weber, J.3
Pivetta, O.H.4
Eigel, A.5
Dworniczak, B.6
-
18
-
-
34247178118
-
Correlación entre las mutaciones del gen CFTR y la expectativa de vida de los pacientes fibroquísticos de América Latina. Actas XXXIII Congreso Argentino de Genética
-
Ibañez C., Pérez M., Pastorale C., Granados P., Keyeux G., Pivetta O.H., et al. Correlación entre las mutaciones del gen CFTR y la expectativa de vida de los pacientes fibroquísticos de América Latina. Actas XXXIII Congreso Argentino de Genética. Basic Appl Genet S-70 (2004)
-
(2004)
Basic Appl Genet
, vol.S-70
-
-
Ibañez, C.1
Pérez, M.2
Pastorale, C.3
Granados, P.4
Keyeux, G.5
Pivetta, O.H.6
-
19
-
-
34247092578
-
-
Prieto L, Chiesa A, Macri C, Gruñeiro-Papendieck L. 1999. Pesquisa neonatal de Fibrosis Quística (FQ): Programa piloto con IRT y DNA. II Congreso Argentino de Neumonología Pediátrica, IX Congreso Latinoamericano de Fibrosis Quística, Buenos Aires, Argentina.
-
-
-
-
20
-
-
0033083982
-
Geographic heterogeneity of four common worldwide cystic fibrosis non F508 mutations in Brazil
-
Raskin S., Phillips J.A., Kaplan G., McLure M., Vnencak-Jones C., and Rozov T. Geographic heterogeneity of four common worldwide cystic fibrosis non F508 mutations in Brazil. Hum Biol 71 (1999) 103-113
-
(1999)
Hum Biol
, vol.71
, pp. 103-113
-
-
Raskin, S.1
Phillips, J.A.2
Kaplan, G.3
McLure, M.4
Vnencak-Jones, C.5
Rozov, T.6
-
21
-
-
34247167254
-
-
Chiba MS, Gomes CET, Silva GP, Bernardino A, Lima C, Zatz M. 2001. Caracteristicas fenotipicas dos pacientes portadores de fibrose cistica. Anais do IX Congresso Brasileiro de Pneumunología Pediatrica, V Congresso da Sociedade Latino Americana de Pneumologia Pediatrica; X Congresso Latino Americano de Fibrose Cistica; IX Jornada Brasileira de Fibrose Cistica; II Jornada Brasileira de Fisioterapia Respiratoria em Pediatria. 28 de septiembre al 3 de octubre 2001 Florianopolis-SC-Brasil.
-
-
-
-
22
-
-
0034090798
-
Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations
-
Bernardino A.L., Ferri A., Passos-Bueno M.R., Kim C.E., Nakaie C.M., Gomes C.E., et al. Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations. Gen Test 4 (2000) 69-74
-
(2000)
Gen Test
, vol.4
, pp. 69-74
-
-
Bernardino, A.L.1
Ferri, A.2
Passos-Bueno, M.R.3
Kim, C.E.4
Nakaie, C.M.5
Gomes, C.E.6
-
23
-
-
0032039748
-
Analysis of the delta F508 mutation in a Brazilian cystic fibrosis population: comparison of pulmonary status of homozygotes with other patients
-
Marostica P.J., Raskin S., and Abreu-e-Silva F.A. Analysis of the delta F508 mutation in a Brazilian cystic fibrosis population: comparison of pulmonary status of homozygotes with other patients. Braz J Med Biol Res 31 (1998) 529-532
-
(1998)
Braz J Med Biol Res
, vol.31
, pp. 529-532
-
-
Marostica, P.J.1
Raskin, S.2
Abreu-e-Silva, F.A.3
-
24
-
-
0030805248
-
Molecular characterization of cystic fibrosis patients in the state of Sao Paulo (Brazil)
-
Parizotto E.A., and Ribeiro AF B.C.S. Molecular characterization of cystic fibrosis patients in the state of Sao Paulo (Brazil). J Med Genet 34 (1997) 877
-
(1997)
J Med Genet
, vol.34
, pp. 877
-
-
Parizotto, E.A.1
Ribeiro AF, B.C.S.2
-
25
-
-
0033118948
-
Cystic fibrosis: low frequency of DF508 mutation in 2 population samples from Rio de Janeiro, Brazil
-
Cabello G.M., Moreira A.F., Horovitz D., Correia P., Santa Rosa A., Llerena Jr. J., et al. Cystic fibrosis: low frequency of DF508 mutation in 2 population samples from Rio de Janeiro, Brazil. Hum Biol 71 (1999) 189-196
-
(1999)
Hum Biol
, vol.71
, pp. 189-196
-
-
Cabello, G.M.1
Moreira, A.F.2
Horovitz, D.3
Correia, P.4
Santa Rosa, A.5
Llerena Jr., J.6
-
26
-
-
0034743399
-
The 3120 + 1G-A splicing mutation in CFTR is common in Brazilian cystic fibrosis patients
-
Cabello G.M., Cabello P.H., Llerena Jr. J., Fernandez O., and Harris A. The 3120 + 1G-A splicing mutation in CFTR is common in Brazilian cystic fibrosis patients. Hum Biol 3 (2001) 403-409
-
(2001)
Hum Biol
, vol.3
, pp. 403-409
-
-
Cabello, G.M.1
Cabello, P.H.2
Llerena Jr., J.3
Fernandez, O.4
Harris, A.5
-
27
-
-
0027674061
-
Frequency of the cystic fibrosis delta F508 mutation in a population from Sao Paulo State, Brazil
-
Martins C.S., Ribeiro F., and Costa F.E. Frequency of the cystic fibrosis delta F508 mutation in a population from Sao Paulo State, Brazil. Braz J Med Biol Res 26 (1993) 1037-1040
-
(1993)
Braz J Med Biol Res
, vol.26
, pp. 1037-1040
-
-
Martins, C.S.1
Ribeiro, F.2
Costa, F.E.3
-
28
-
-
0037385203
-
CFTR gene: molecular analysis in patients from South Brazil
-
Streit C., Burlamaque-Neto A.C., de Abreu e Silva F., Giugliani R., and Saraiva Pereira M.L. CFTR gene: molecular analysis in patients from South Brazil. Mol Genet Metab 78 (2003) 259-264
-
(2003)
Mol Genet Metab
, vol.78
, pp. 259-264
-
-
Streit, C.1
Burlamaque-Neto, A.C.2
de Abreu e Silva, F.3
Giugliani, R.4
Saraiva Pereira, M.L.5
-
29
-
-
0141429177
-
CFTR molecular analysis reveals infrequent allele frequencies in nine cystic fibrosis patients from Sao Paulo State, Brazil
-
Goloni-Bertollo E.M., Rossit A.R.B., Batista J., Junior S., Fett-Conte A.C., and Raskin S. CFTR molecular analysis reveals infrequent allele frequencies in nine cystic fibrosis patients from Sao Paulo State, Brazil. Hum Biol 3 (2003) 393-398
-
(2003)
Hum Biol
, vol.3
, pp. 393-398
-
-
Goloni-Bertollo, E.M.1
Rossit, A.R.B.2
Batista, J.3
Junior, S.4
Fett-Conte, A.C.5
Raskin, S.6
-
30
-
-
0027998620
-
CFTR mutations in Chilean cystic fibrosis patients
-
Rios T., Orellana O., Aspillaga M., Avendaño Y., Largo Y., and Riveros N. CFTR mutations in Chilean cystic fibrosis patients. Hum Genet 94 (1994) 291-294
-
(1994)
Hum Genet
, vol.94
, pp. 291-294
-
-
Rios, T.1
Orellana, O.2
Aspillaga, M.3
Avendaño, Y.4
Largo, Y.5
Riveros, N.6
-
31
-
-
0346677882
-
Estudio clínico-genético molecular de la fibrosis quística en la V Región, Chile
-
Molina G., Gonzalez F.J., Cave R., Cornejo de M., Navarro S., Deglin M., et al. Estudio clínico-genético molecular de la fibrosis quística en la V Región, Chile (Clinical and molecular genetic study of cystic fibrosis in the 5th Region of Chile). Rev Méd Chile 130 (2002) 850-858
-
(2002)
Rev Méd Chile
, vol.130
, pp. 850-858
-
-
Molina, G.1
Gonzalez, F.J.2
Cave, R.3
Cornejo de, M.4
Navarro, S.5
Deglin, M.6
-
32
-
-
0346678536
-
Correlation between phenotype and genotype in a group of patients with cystic fibrosis
-
Navarro H., Kolbach M., Repetto G., Guiraldes E., Harris P., and Foradori A. Correlation between phenotype and genotype in a group of patients with cystic fibrosis. Rev Méd Chile 130 (2002) 475-481
-
(2002)
Rev Méd Chile
, vol.130
, pp. 475-481
-
-
Navarro, H.1
Kolbach, M.2
Repetto, G.3
Guiraldes, E.4
Harris, P.5
Foradori, A.6
-
33
-
-
0035432167
-
Identification of mutation in the gene cystic fibrosis transmembrane regulator (CFTR) in Chilean patients with cystic fibrosis
-
Repetto G., Poggi H., Harris P., Navarro H., Sanchez I., Guiraldes E., et al. Identification of mutation in the gene cystic fibrosis transmembrane regulator (CFTR) in Chilean patients with cystic fibrosis. Rev Med Chile 129 (2001) 841-847
-
(2001)
Rev Med Chile
, vol.129
, pp. 841-847
-
-
Repetto, G.1
Poggi, H.2
Harris, P.3
Navarro, H.4
Sanchez, I.5
Guiraldes, E.6
-
34
-
-
19244378402
-
Cystic Fibrosis gene mutation in three Latin American countries
-
Restrepo C.M., Pineda L., Rojas-Martínez A., Gutiérrez C.A., Gómez Y., Borjas L., et al. Cystic Fibrosis gene mutation in three Latin American countries. Am J Med Genet 91 (2000) 277-279
-
(2000)
Am J Med Genet
, vol.91
, pp. 277-279
-
-
Restrepo, C.M.1
Pineda, L.2
Rojas-Martínez, A.3
Gutiérrez, C.A.4
Gómez, Y.5
Borjas, L.6
-
35
-
-
0037911528
-
Cystic fibrosis mutations in Costa Rica
-
Venegas P.B., Novak J.M., Oscar C.A., Sanchez F.L., Gutierrez I.G., Rivera J.M., et al. Cystic fibrosis mutations in Costa Rica. Hum Biol 75 (2003) 179-188
-
(2003)
Hum Biol
, vol.75
, pp. 179-188
-
-
Venegas, P.B.1
Novak, J.M.2
Oscar, C.A.3
Sanchez, F.L.4
Gutierrez, I.G.5
Rivera, J.M.6
-
36
-
-
0028819107
-
Frequency of delta-F508 mutation and XV2C/KM19 haplotypes in Cuban cystic fibrosis families
-
Collazo T., Magarino C., Chávez R., Suardez B., Gispert S., Gómez M., et al. Frequency of delta-F508 mutation and XV2C/KM19 haplotypes in Cuban cystic fibrosis families. Hum Hered 45 (1995) 55-57
-
(1995)
Hum Hered
, vol.45
, pp. 55-57
-
-
Collazo, T.1
Magarino, C.2
Chávez, R.3
Suardez, B.4
Gispert, S.5
Gómez, M.6
-
37
-
-
34247161453
-
-
Merino M, Schollen E, Matthijs G, Dequeker G, Martinez E, Tapia M, et al. 1999. Estudios moleculares de fibrosis quística en pacientes de Ecuador. Actas del II Congreso Argentino de Neumonología Pediátrica. IX Congreso Latinoamericano de Fibrosis Quística. 24 al 27 de noviembre de 1999. Buenos Aires, Argentina.
-
-
-
-
38
-
-
0032589290
-
The DeltaF508 mutation in Ecuador, South America
-
Paz-y-Mino C., Perez J.C., Burgos R., Davalos M.V., and Leone P.E. The DeltaF508 mutation in Ecuador, South America. Hum Mutat 14 (1999) 348-350
-
(1999)
Hum Mutat
, vol.14
, pp. 348-350
-
-
Paz-y-Mino, C.1
Perez, J.C.2
Burgos, R.3
Davalos, M.V.4
Leone, P.E.5
-
39
-
-
0030980906
-
Analysis of 16 cystic fibrosis mutations in Mexican patients
-
Villalobos-Torres C., Rojas-Martínez A., Villarreal-Castellanos E., Cantu J.M., Sanchez-Anzaldo F.J., Saiki R.K., et al. Analysis of 16 cystic fibrosis mutations in Mexican patients. Am J Med Genet 69 (1997) 380-382
-
(1997)
Am J Med Genet
, vol.69
, pp. 380-382
-
-
Villalobos-Torres, C.1
Rojas-Martínez, A.2
Villarreal-Castellanos, E.3
Cantu, J.M.4
Sanchez-Anzaldo, F.J.5
Saiki, R.K.6
-
40
-
-
34247170107
-
-
Luzardo G, Crispino B, Mimbacas A, Martinez L, Cardoso H. 1999. Análisis de las frecuencias de las mutaciones de fibrosis quística según criterios diagnósticos en una muestra de la población Uruguaya. II Congreso Argentino de Neumonología Pediátrica. IX Congreso Latinoamericano de Fibrosis Quística. Buenos Aires, Argentina.
-
-
-
-
41
-
-
2342439411
-
Cystic fibrosis in Uruguay
-
Luzardo G., Aznarez I., Crispino B., Mimbacas A., Martínez L., Poggio R., et al. Cystic fibrosis in Uruguay. Genet Mol Res 1 (2002) 32-38
-
(2002)
Genet Mol Res
, vol.1
, pp. 32-38
-
-
Luzardo, G.1
Aznarez, I.2
Crispino, B.3
Mimbacas, A.4
Martínez, L.5
Poggio, R.6
-
42
-
-
34247106837
-
-
Alvarado J., Acosta L., Carrasquel B., Lugo Z. 2000. Fibrosis Quística. Estudio de 41 Pacientes-Hospital de Niños "J.M. de los Ríos" Acta Otorrinolaringológica 12, Venezuela.
-
-
-
-
43
-
-
34247112007
-
-
Schneider S, Roessli D, Excoffier L. 2000. ARLEQUIN ver 2.000. A software for population genetics data analysis. http://anthro.unige.ch/arlequin.
-
-
-
-
44
-
-
34247116137
-
-
Langella O. Populations 2002; 1.2.28, CNRS UPR9034. http://www.cnrs-gif.fr/pge.
-
-
-
-
45
-
-
34247149497
-
-
Page R 2001; Tree View (Win32) 1.6.5.http://www.taxonomy.zoology.gla.ac.uk/rod/rod.html.
-
-
-
-
46
-
-
34247133192
-
Particular aspects of the molecular basis of cystic fibrosis in Colombia
-
Keyeux G., Bienvenu T., Rodas C., Garavito P., Sanchez D., Stand I., et al. Particular aspects of the molecular basis of cystic fibrosis in Colombia. Am J Hum Genet 4 (1997) A202
-
(1997)
Am J Hum Genet
, vol.4
-
-
Keyeux, G.1
Bienvenu, T.2
Rodas, C.3
Garavito, P.4
Sanchez, D.5
Stand, I.6
-
47
-
-
3242718811
-
Mutations in CFTR gene and clinical correlation in argentine patients with congenital bilateral absence of the vas deferens
-
Levy E.M., Granados P., Rawe V., Brugo Olmedo S., Luna M.C., Cafferata E., et al. Mutations in CFTR gene and clinical correlation in argentine patients with congenital bilateral absence of the vas deferens. Medicina (Buenos Aires) 64 (2004) 213-218
-
(2004)
Medicina (Buenos Aires)
, vol.64
, pp. 213-218
-
-
Levy, E.M.1
Granados, P.2
Rawe, V.3
Brugo Olmedo, S.4
Luna, M.C.5
Cafferata, E.6
-
48
-
-
0004226825
-
-
Sinauer associates, Inc. Sunderland, Massachusetts
-
Hartl D. Principles of population genetics (1997), Sinauer associates, Inc. Sunderland, Massachusetts
-
(1997)
Principles of population genetics
-
-
Hartl, D.1
-
49
-
-
0033941783
-
mtDNA affinities of the peoples of North-Central Mexico
-
Green L.D., Derr J.N., and Knight A. mtDNA affinities of the peoples of North-Central Mexico. Am J Hum Genet 66 (2000) 989-998
-
(2000)
Am J Hum Genet
, vol.66
, pp. 989-998
-
-
Green, L.D.1
Derr, J.N.2
Knight, A.3
-
50
-
-
0037309485
-
Mitochondrial DNA studies show asymmetrical Amerindian admixture in Afro-Colombian and Mestizo populations
-
Rodas C., Gelvez G., and Keyeux. Mitochondrial DNA studies show asymmetrical Amerindian admixture in Afro-Colombian and Mestizo populations. Hum Biol 75 (2003) 13-30
-
(2003)
Hum Biol
, vol.75
, pp. 13-30
-
-
Rodas, C.1
Gelvez, G.2
Keyeux3
-
52
-
-
34247106378
-
Case report of a Thai male cystic fibrosis patient with the 1898 + 1G > T splicing mutation in the CFTR gene: a review of East Asian cases
-
Mutation in Brief # 196 Online
-
Suwanjutha S., Huang N.N., Wattanasirichaigoon D., Sura T., Harris A., and Macek Jr. M. Case report of a Thai male cystic fibrosis patient with the 1898 + 1G > T splicing mutation in the CFTR gene: a review of East Asian cases. Hum Mutat (1998) 1-4 Mutation in Brief # 196 Online
-
(1998)
Hum Mutat
, pp. 1-4
-
-
Suwanjutha, S.1
Huang, N.N.2
Wattanasirichaigoon, D.3
Sura, T.4
Harris, A.5
Macek Jr., M.6
-
53
-
-
0033913365
-
Novel cystic fibrosis mutation (2215insG) in two adolescent Taiwanese siblings
-
Wu C.L., Shu S.G., Zielinski J., Chiang C.D., and Tsui L.C. Novel cystic fibrosis mutation (2215insG) in two adolescent Taiwanese siblings. J Formos Med Assoc 99 (2000) 564-567
-
(2000)
J Formos Med Assoc
, vol.99
, pp. 564-567
-
-
Wu, C.L.1
Shu, S.G.2
Zielinski, J.3
Chiang, C.D.4
Tsui, L.C.5
-
54
-
-
0036258208
-
Cystic fibrosis: a worldwide analysis of CFTR mutations-correlation with incidence data and application to screening
-
Bobadilla J.L., Macek M., Fine J.P., and Farell P.M. Cystic fibrosis: a worldwide analysis of CFTR mutations-correlation with incidence data and application to screening. Hum Mutat 19 (2002) 575-606
-
(2002)
Hum Mutat
, vol.19
, pp. 575-606
-
-
Bobadilla, J.L.1
Macek, M.2
Fine, J.P.3
Farell, P.M.4
-
55
-
-
19244364425
-
First report of CFTR mutations in black cystic fibrosis patients of southern African origin
-
Carles S., Desgeorges M., Goldman A., Thiart R., Guittard C., Kitazos C.A., et al. First report of CFTR mutations in black cystic fibrosis patients of southern African origin. J Med Genet 33 (1996) 802-804
-
(1996)
J Med Genet
, vol.33
, pp. 802-804
-
-
Carles, S.1
Desgeorges, M.2
Goldman, A.3
Thiart, R.4
Guittard, C.5
Kitazos, C.A.6
-
56
-
-
16944366526
-
Identification of common cystic fibrosis mutations in African-Americans with cystic fibrosis increases the detection rate to 75%
-
Macek M., Mackova A., Hamosh A., Hilman B.C., Selden R.F., Lucotte G., et al. Identification of common cystic fibrosis mutations in African-Americans with cystic fibrosis increases the detection rate to 75%. Am J Hum Genet 60 (1997) 1122-1127
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1122-1127
-
-
Macek, M.1
Mackova, A.2
Hamosh, A.3
Hilman, B.C.4
Selden, R.F.5
Lucotte, G.6
-
57
-
-
0032929774
-
Cystic fibrosis carrier frequencies in populations of African origin
-
Padoa C., Goldman A., Jenkins T., and Ramsay M. Cystic fibrosis carrier frequencies in populations of African origin. J Med Genet 36 (1999) 41-44
-
(1999)
J Med Genet
, vol.36
, pp. 41-44
-
-
Padoa, C.1
Goldman, A.2
Jenkins, T.3
Ramsay, M.4
|