-
2
-
-
0344325111
-
-
R001 (available from
-
Van Camp G, Smith RJH. R001 (available from: http://www.uia.ac.be/dnalab/hhh).
-
-
-
Van Camp, G.1
Smith, R.J.H.2
-
3
-
-
12644276408
-
Linkage of DFNB1 to non-syndromic neurosensory autosomal recessive deafness in Mediterranean families
-
Gasparini P, Estivill X, Volpini V et al. Linkage of DFNB1 to non-syndromic neurosensory autosomal recessive deafness in Mediterranean families. Eur J Hum Genet 1997: 5: 83-88.
-
(1997)
Eur. J. Hum. Genet.
, vol.5
, pp. 83-88
-
-
Gasparini, P.1
Estivill, X.2
Volpini, V.3
-
4
-
-
0031007349
-
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
-
Kelsell DP, Dunlop J, Stevens HP et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature 1997: 387: 80-83.
-
(1997)
Nature
, vol.387
, pp. 80-83
-
-
Kelsell, D.P.1
Dunlop, J.2
Stevens, H.P.3
-
5
-
-
9844245885
-
Connexin 26 mutations associated with the most common form of non-syndromic neurosensory autosomal deafness (DFNB1) in Mediterraneans
-
Zelante L, Gasparini P, Estivill X et al. Connexin 26 mutations associated with the most common form of non-syndromic neurosensory autosomal deafness (DFNB1) in Mediterraneans. Hum Mol Genet 1997: 6: 1605-1609.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1605-1609
-
-
Zelante, L.1
Gasparini, P.2
Estivill, X.3
-
6
-
-
17544402026
-
High carrier frequency of the 35delG deafness mutation in European populations. Genetic analysis consortium of GJB2 35delG
-
Gasparini P, Rabionet R, Barbujani G et al. High carrier frequency of the 35delG deafness mutation in European populations. Genetic analysis consortium of GJB2 35delG. Eur J Hum Genet 2000: 8: 19-23.
-
(2000)
Eur. J. Hum. Genet.
, vol.8
, pp. 19-23
-
-
Gasparini, P.1
Rabionet, R.2
Barbujani, G.3
-
7
-
-
0034876240
-
Meta-analysis of GJB2 mutation 35delG frequencies in Europe
-
Lucotte G, Mercier G. Meta-analysis of GJB2 mutation 35delG frequencies in Europe. Genet Test 2001: 5: 149-152.
-
(2001)
Genet. Test.
, vol.5
, pp. 149-152
-
-
Lucotte, G.1
Mercier, G.2
-
8
-
-
0034881345
-
A common founder for the 35delG GJB gene mutation in connexin 26 hearing impairment
-
Van Laer L, Coucke P, Mueller RF et al. A common founder for the 35delG GJB gene mutation in connexin 26 hearing impairment. J Med Genet 2001: 38: 515-518.
-
(2001)
J. Med. Genet.
, vol.38
, pp. 515-518
-
-
Van Laer, L.1
Coucke, P.2
Mueller, R.F.3
-
9
-
-
0035129646
-
PCR test for diagnosis of the common GJB2-35delG mutation on dried blood spots and determination of the carrier frequency in France
-
Lucotte G, Bathelier C, Champenois T. PCR test for diagnosis of the common GJB2-35delG mutation on dried blood spots and determination of the carrier frequency in France. Mol Cell Probes 2001: 15: 57-59.
-
(2001)
Mol. Cell Probes
, vol.15
, pp. 57-59
-
-
Lucotte, G.1
Bathelier, C.2
Champenois, T.3
-
10
-
-
0036023041
-
Haplotypes of the Y chromosome in Corsica
-
[in French]
-
Lucotte G, Pinna A, Mercier G. Haplotypes of the Y chromosome in Corsica. CR Biol 2002: 325: 191-196 [in French].
-
(2002)
CR Biol.
, vol.325
, pp. 191-196
-
-
Lucotte, G.1
Pinna, A.2
Mercier, G.3
-
11
-
-
0032492217
-
Connexin-26 mutations in sporadic and inherited sensorineural deafness
-
Estivill X, Fortina P, Surrey S et al. Connexin-26 mutations in sporadic and inherited sensorineural deafness. Lancet 1998: 351: 394-398.
-
(1998)
Lancet
, vol.351
, pp. 394-398
-
-
Estivill, X.1
Fortina, P.2
Surrey, S.3
-
12
-
-
0033014505
-
High prevalence in the Greek population of the 35delG mutation in the connexin 26 gene causing prelingual deafness
-
Antoniadi T, Rabionet R, Kroupis C et al. High prevalence in the Greek population of the 35delG mutation in the connexin 26 gene causing prelingual deafness. Clin Genet 1999: 55: 581-582.
-
(1999)
Clin. Genet.
, vol.55
, pp. 581-582
-
-
Antoniadi, T.1
Rabionet, R.2
Kroupis, C.3
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