-
2
-
-
0026663506
-
Genetic deafness
-
Reardon W: Genetic deafness. J Med Genet 1992;29:521-526.
-
(1992)
J Med Genet
, vol.29
, pp. 521-526
-
-
Reardon, W.1
-
4
-
-
0028249690
-
A non-syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q
-
Guilford P, Arab SB, Blanchard S, Levilliers J, Weissenbach J, Belkahia A, Petit C: A non-syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q. Nature Genet 1994;6:24-28.
-
(1994)
Nature Genet
, vol.6
, pp. 24-28
-
-
Guilford, P.1
Arab, S.B.2
Blanchard, S.3
Levilliers, J.4
Weissenbach, J.5
Belkahia, A.6
Petit, C.7
-
5
-
-
0028306509
-
A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene
-
Guilford P, Ayadi H, Blanchard S, Chaib H, Le Paslier D, Weissenbach J, Drira M, Petit C: A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene. Hum Mol Genet 1994;3:989-993.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 989-993
-
-
Guilford, P.1
Ayadi, H.2
Blanchard, S.3
Chaib, H.4
Le Paslier, D.5
Weissenbach, J.6
Drira, M.7
Petit, C.8
-
6
-
-
0028836920
-
A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17
-
Friedman TB, Liang Y, Weber JL, Hinnant JT, Barber TD, Winata S, Arhya IN, Asher JH Jr: A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17. Nature Genet 1995;9:86-91.
-
(1995)
Nature Genet
, vol.9
, pp. 86-91
-
-
Friedman, T.B.1
Liang, Y.2
Weber, J.L.3
Hinnant, J.T.4
Barber, T.D.5
Winata, S.6
Arhya, I.N.7
Asher Jr., J.H.8
-
7
-
-
0029145428
-
Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population
-
Baldwin CT, Farrer LA, Weiss S, De Stefano AL, Adair R, Franklyn B, Kidd KK, Korostishevsky M, Bonne-Tamir B: Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population. Hum Mol Genet 1995;4:1637-1642.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1637-1642
-
-
Baldwin, C.T.1
Farrer, L.A.2
Weiss, S.3
De Stefano, A.L.4
Adair, R.5
Franklyn, B.6
Kidd, K.K.7
Korostishevsky, M.8
Bonne-Tamir, B.9
-
8
-
-
0029086703
-
Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q
-
Fukushima K, Arabandi R, Srisailapathy CRS, Ni L, Chen A, O'Neill M, Van Camp G, Coucke P, Smith SD, Kenyon JB, Jain P, Wilcox ER, Zbar RIS, Smith RJH: Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q. Hum Mol Genet 1995;4:1643-1648.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1643-1648
-
-
Fukushima, K.1
Arabandi, R.2
Srisailapathy, C.R.S.3
Ni, L.4
Chen, A.5
O'Neill, M.6
Van Camp, G.7
Coucke, P.8
Smith, S.D.9
Kenyon, J.B.10
Jain, P.11
Wilcox, E.R.12
Zbar, R.I.S.13
Smith, R.J.H.14
-
9
-
-
0028862795
-
An autosomal recessive non-syndromic form of sensorineural hearing loss maps to 3p-DFNB6
-
Fukushima K, Arabandi R, Srisailapathy CRS, Ni L, Wayne S, O'Neill ME, Van Camp G, Coucke P, Jain P, Wilcox ER, Smith SD, Kenyon JB, Zbar RIS, Smith RJH: An autosomal recessive non-syndromic form of sensorineural hearing loss maps to 3p-DFNB6. Genome Res 1995;5:305-308.
-
(1995)
Genome Res
, vol.5
, pp. 305-308
-
-
Fukushima, K.1
Arabandi, R.2
Srisailapathy, C.R.S.3
Ni, L.4
Wayne, S.5
O'Neill, M.E.6
Van Camp, G.7
Coucke, P.8
Jain, P.9
Wilcox, E.R.10
Smith, S.D.11
Kenyon, J.B.12
Zbar, R.I.S.13
Smith, R.J.H.14
-
10
-
-
0028837681
-
A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus
-
Jain PK, Fukushima K, Deshmukh D, Arabandi R, Thomas E, Kumar S, Lalwani AK, Kumar S, Ploplis B, Skarka H, Srisailapathy CRS, Wayne S, Zbar RIS, Verma IC, Smith RJH, Wilcox ER: A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus. Hum Mol Genet 1995;4:2391-2394.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2391-2394
-
-
Jain, P.K.1
Fukushima, K.2
Deshmukh, D.3
Arabandi, R.4
Thomas, E.5
Kumar, S.6
Lalwani, A.K.7
Kumar, S.8
Ploplis, B.9
Skarka, H.10
Srisailapathy, C.R.S.11
Wayne, S.12
Zbar, R.I.S.13
Verma, I.C.14
Smith, R.J.H.15
Wilcox, E.R.16
-
11
-
-
0030070163
-
Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21 q22 in large consanguineous kindred from Pakistan
-
Veske A, Oehlmann R, Younus F, Mohyuddin A, Muller-Myhsok B, Qasim Mehdi S, Gal A: Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21 q22 in large consanguineous kindred from Pakistan. Hum Mol Genet 1996;5:165-168.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 165-168
-
-
Veske, A.1
Oehlmann, R.2
Younus, F.3
Mohyuddin, A.4
Muller-Myhsok, B.5
Qasim Mehdi, S.6
Gal, A.7
-
12
-
-
0030047197
-
A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23
-
Chaib H, Place C, Salem N, Chardenoux S, Vincent C, Weissenbach J, El-Zir E, Loiselet J, Petit C: A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23. Hum Mol Genet 1996;5: 155-158.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 155-158
-
-
Chaib, H.1
Place, C.2
Salem, N.3
Chardenoux, S.4
Vincent, C.5
Weissenbach, J.6
El-Zir, E.7
Loiselet, J.8
Petit, C.9
-
13
-
-
0029883986
-
Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21 q22.3
-
Bonne'-Tamir B, DeStefano AL, Briggs CE, Adair R, Franklyn B, Weiss S, Korostishevsky M, Frydman M, Baldwin CT, Farrer LA: Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21 q22.3. Am J Hum Genet 1996;58:1254-1259.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1254-1259
-
-
Bonne'-Tamir, B.1
DeStefano, A.L.2
Briggs, C.E.3
Adair, R.4
Franklyn, B.5
Weiss, S.6
Korostishevsky, M.7
Frydman, M.8
Baldwin, C.T.9
Farrer, L.A.10
-
14
-
-
0030054738
-
Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22
-
Chaib H, Place C, Salem N, Salem N, Dode' C, Chardenoux S, Weissenbach J, El-Zir E, Loiselet J, Petit C: Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22. Hum Mol Genet 1996;5:1061-1064.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1061-1064
-
-
Chaib, H.1
Place, C.2
Salem, N.3
Salem, N.4
Dode, C.5
Chardenoux, S.6
Weissenbach, J.7
El-Zir, E.8
Loiselet, J.9
Petit, C.10
-
15
-
-
0029166965
-
The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian population
-
Maw MA, Allen Powell DR, Goodey RJ, Stewart IA, Nancarrow DJ, Hayward N, McKinlay Gardner RJ: The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian population. Am J Hum Genet 1995; 57:629-635.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 629-635
-
-
Maw, M.A.1
Allen Powell, D.R.2
Goodey, R.J.3
Stewart, I.A.4
Nancarrow, D.J.5
Hayward, N.6
McKinlay Gardner, R.J.7
-
16
-
-
9044254521
-
Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175
-
Brown KA, Janjua AH, Karbani G, Parry G, Noble A, Crockford G, Bishop DT, Newton VE, Markham AF, Mueller RF: Linkage studies of non-syndromic recessive deafness (NSRD) in a family originating from the Mirpur region of Pakistan maps DFNB1 centromeric to D13S175. Hum Mol Genet 1996;5: 169-173.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 169-173
-
-
Brown, K.A.1
Janjua, A.H.2
Karbani, G.3
Parry, G.4
Noble, A.5
Crockford, G.6
Bishop, D.T.7
Newton, V.E.8
Markham, A.F.9
Mueller, R.F.10
-
18
-
-
0020049449
-
Construction of human gene libraries from small amounts of peripheral blood: Analyses of β-like globin genes
-
Poncz M, Solowiejzcyk D, Harpel B, Mory Y, Schwartz E, Surrey S: Construction of human gene libraries from small amounts of peripheral blood: Analyses of β-like globin genes. Hemoglobin 1982;6:27-36.
-
(1982)
Hemoglobin
, vol.6
, pp. 27-36
-
-
Poncz, M.1
Solowiejzcyk, D.2
Harpel, B.3
Mory, Y.4
Schwartz, E.5
Surrey, S.6
-
19
-
-
0023502864
-
Chemical synthesis of deoxyoligonucleotides by the phosphoramidite method
-
Caruthers MH, Barone AD, Beaucage SL, Dodds DR, Fisher EF, McBride LJ, Matteucci M, Stabinsky Z, Tang J-Y: Chemical synthesis of deoxyoligonucleotides by the phosphoramidite method. Methods Enzymol 1987;154: 287-313.
-
(1987)
Methods Enzymol
, vol.154
, pp. 287-313
-
-
Caruthers, M.H.1
Barone, A.D.2
Beaucage, S.L.3
Dodds, D.R.4
Fisher, E.F.5
McBride, L.J.6
Matteucci, M.7
Stabinsky, Z.8
Tang, J.-Y.9
-
20
-
-
12644252933
-
Synthesis of fluorescent dye-labeled oligonucleotides for use as primers in fluorescent-based DNA sequencing
-
Applied Biosystems, Inc: Synthesis of fluorescent dye-labeled oligonucleotides for use as primers in fluorescent-based DNA sequencing. ABI User Bull 1991;11:6-9.
-
(1991)
ABI User Bull
, vol.11
, pp. 6-9
-
-
-
21
-
-
0026736249
-
Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms
-
Hudson TJ, Engelstein M, Lee MK, Ho EC, Rubenfield MJ, Adams CP, Housman DE, Dracopoli NC: Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms. Genomics 1992;13:622-629.
-
(1992)
Genomics
, vol.13
, pp. 622-629
-
-
Hudson, T.J.1
Engelstein, M.2
Lee, M.K.3
Ho, E.C.4
Rubenfield, M.J.5
Adams, C.P.6
Housman, D.E.7
Dracopoli, N.C.8
-
22
-
-
0026446099
-
A second-generation linkage map of the human genome
-
Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseiz G, Lathrop M: A second-generation linkage map of the human genome. Nature 1992;359:794-801.
-
(1992)
Nature
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morissette, J.5
Millasseau, P.6
Vaysseiz, G.7
Lathrop, M.8
-
23
-
-
0027450804
-
A microsatellite genetic linkage map of human chromosome 13
-
Petrukhin KE, Speer MC, Cayanis E, de Fatima Bonaldo M, Tantravahi U, Scares MB, Fischer SG, Warburton D, Gilliam TC, Ott J: A microsatellite genetic linkage map of human chromosome 13. Genomics 1993;15:76-85.
-
(1993)
Genomics
, vol.15
, pp. 76-85
-
-
Petrukhin, K.E.1
Speer, M.C.2
Cayanis, E.3
De Fatima Bonaldo, M.4
Tantravahi, U.5
Scares, M.B.6
Fischer, S.G.7
Warburton, D.8
Gilliam, T.C.9
Ott, J.10
-
24
-
-
0027366195
-
Faster sequential genetic linkage computations
-
Cottingam R, Idury R, Schaffer A: Faster sequential genetic linkage computations. Am J Hum Genet 1993;53:252-263.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 252-263
-
-
Cottingam, R.1
Idury, R.2
Schaffer, A.3
-
25
-
-
0021850103
-
Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
-
Lathrop GM, Lalouel JM, Julier C, Ott J: Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination. Am J Hum Genet 1984;37:482-498.
-
(1984)
Am J Hum Genet
, vol.37
, pp. 482-498
-
-
Lathrop, G.M.1
Lalouel, J.M.2
Julier, C.3
Ott, J.4
|