-
2
-
-
0030999545
-
Genetic variability in two Brazilian ethnic groups: A comparison of mitochondrial and protein data
-
Bortolini, M.C., F.M. Salzano, M.A. Zago et al. 1997. Genetic variability in two Brazilian ethnic groups: A comparison of mitochondrial and protein data. Am. J. Phys. Anthropol. 103:147-156.
-
(1997)
Am. J. Phys. Anthropol.
, vol.103
, pp. 147-156
-
-
Bortolini, M.C.1
Salzano, F.M.2
Zago, M.A.3
-
3
-
-
0000674295
-
Brazilian Indian/non-Indian interactions and their effects
-
Callegari-Jacques, S.M., and F.M. Salzano. 1999. Brazilian Indian/non-Indian interactions and their effects. Ciênc. Cult. 51:166-174.
-
(1999)
Ciênc. Cult.
, vol.51
, pp. 166-174
-
-
Callegari-Jacques, S.M.1
Salzano, F.M.2
-
5
-
-
17544402026
-
High carrier frequency of the 35delG deafness mutation in European populations
-
Gasparini, P., R. Rabionet, G. Barbujani et al. 2000. High carrier frequency of the 35delG deafness mutation in European populations. Eur. J. Hum. Genet. 8:19-23.
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 19-23
-
-
Gasparini, P.1
Rabionet, R.2
Barbujani, G.3
-
6
-
-
0033575109
-
Carrier raters in the Midwestern United States for GJB2 mutations causing inherited deafness
-
Green, G.E., D.A. Scott, J.M. McDonald et al. 1999. Carrier raters in the Midwestern United States for GJB2 mutations causing inherited deafness. J Am. Med. Assoc. 281(23):2,211-2,216.
-
(1999)
J Am. Med. Assoc.
, vol.281
, Issue.23
-
-
Green, G.E.1
Scott, D.A.2
McDonald, J.M.3
-
7
-
-
0031007349
-
Connexin 26 mutations in hereditary nonsyndromic sensorineural deafness
-
Kelsell, D.P., J. Dunlop, H.P. Stevens et al. 1997. Connexin 26 mutations in hereditary nonsyndromic sensorineural deafness. Nature 387:80-83.
-
(1997)
Nature
, vol.387
, pp. 80-83
-
-
Kelsell, D.P.1
Dunlop, J.2
Stevens, H.P.3
-
8
-
-
0036590216
-
Deafness resulting from mutations in the GJB2 (connexin 26) gene in Brazilian patients
-
Oliveira, C.A., A.T. Maciel-Guerra, and E.L. Sartorato. 2002. Deafness resulting from mutations in the GJB2 (connexin 26) gene in Brazilian patients. Clin. Genet. 61:354-358.
-
(2002)
Clin. Genet.
, vol.61
, pp. 354-358
-
-
Oliveira, C.A.1
Maciel-Guerra, A.T.2
Sartorato, E.L.3
-
10
-
-
0033819276
-
Determination of the frequency of 35delG allele in Brazilian neonates
-
Sartorato, E.L., E. Gottardi, C.A. Oliveira et al. 2000. Determination of the frequency of 35delG allele in Brazilian neonates. Clin. Genet. 58:339-340.
-
(2000)
Clin. Genet.
, vol.58
, pp. 339-340
-
-
Sartorato, E.L.1
Gottardi, E.2
Oliveira, C.A.3
-
11
-
-
7144228618
-
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss
-
Scott, D.A., M.L. Kraft, R. Carmi et al. 1998. Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss. Hum. Mutat. 11:387-394.
-
(1998)
Hum. Mutat.
, vol.11
, pp. 387-394
-
-
Scott, D.A.1
Kraft, M.L.2
Carmi, R.3
-
12
-
-
0001159216
-
A surdez evitável: Predominância de fatores ambientais na etiologia da surdez neurossensorial profunda
-
Simões, A.M., and A.T. Maciel-Guerra. 1992. A surdez evitável: Predominância de fatores ambientais na etiologia da surdez neurossensorial profunda. J. Pediatr. 68:254-257.
-
(1992)
J. Pediatr.
, vol.68
, pp. 254-257
-
-
Simões, A.M.1
Maciel-Guerra, A.T.2
-
13
-
-
0032281841
-
Human races: A genetic and evolutionary perspective
-
Templeton, A.R. 1998. Human races: A genetic and evolutionary perspective. Am. Anthropol. 100:632-650.
-
(1998)
Am. Anthropol.
, vol.100
, pp. 632-650
-
-
Templeton, A.R.1
|