-
1
-
-
85192663033
-
Usher syndrome in Jewish Morroccan families
-
Adato A, Kalinski H, Pel-Or Y, Korostishevsky M, and Bonné-Tamir B (1996) Usher syndrome in Jewish Morroccan families. Cell. Pharm. 3:231-236.
-
(1996)
Cell. Pharm.
, vol.3
, pp. 231-236
-
-
Adato, A.1
Kalinski, H.2
Pel-Or, Y.3
Korostishevsky, M.4
Bonné-Tamir, B.5
-
2
-
-
0030869710
-
Mutation profile of all 49 exons of the human myosin VII a gene, and haplotype analysis in usher 1B families from diverse origins
-
in press
-
Adato A, Weil D, Kalinski H, Pel-Or Y, Ayadi H, Petit C, Korostishevsky M, and Bonné-Tamir B (1997) Mutation profile of all 49 exons of the human myosin VII A gene, and haplotype analysis in usher 1B families from diverse origins. Am. J. Hum. Genet, (in press).
-
(1997)
Am. J. Hum. Genet
-
-
Adato, A.1
Weil, D.2
Kalinski, H.3
Pel-Or, Y.4
Ayadi, H.5
Petit, C.6
Korostishevsky, M.7
Bonné-Tamir, B.8
-
3
-
-
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, and Bonné-Tamir B (1995) Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population. Hum. Mol. Genet. 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
Bonné-Tamir, B.9
-
4
-
-
0028113076
-
RPS2 of arabidopsis thaliana: A leucine-rich repeat class of plant disease resistance genes
-
Bent AF, Kunkel BN, Dahlbeck D, Brown KL, Schmidt R, Giraudat J, Leung J, and Staskawicz BJ (1994) RPS2 of arabidopsis thaliana: A leucine-rich repeat class of plant disease resistance genes. Science 265: 1856-1860.
-
(1994)
Science
, vol.265
, pp. 1856-1860
-
-
Bent, A.F.1
Kunkel, B.N.2
Dahlbeck, D.3
Brown, K.L.4
Schmidt, R.5
Giraudat, J.6
Leung, J.7
Staskawicz, B.J.8
-
5
-
-
33646224271
-
The Samaritans: A demographic study
-
Bonné B (1963) The Samaritans: A demographic study. Hum. Biol. 35:61-89.
-
(1963)
Hum. Biol.
, vol.35
, pp. 61-89
-
-
Bonné, B.1
-
6
-
-
84981818619
-
Genes and phenotypes in the Samaritan isolate
-
Bonné B (1996a) Genes and phenotypes in the Samaritan isolate. Am. J. Phys. Anthropol. 24:1-20.
-
(1996)
Am. J. Phys. Anthropol.
, vol.24
, pp. 1-20
-
-
Bonné, B.1
-
7
-
-
0013893580
-
Are there Hebrews left?
-
Bonné B (1996b) Are there Hebrews left? Am. J. Phys. Anthropol. 24:135-145.
-
(1996)
Am. J. Phys. Anthropol.
, vol.24
, pp. 135-145
-
-
Bonné, B.1
-
8
-
-
1542314005
-
The Samaritans: A living ancient isolate
-
AW Eriksson et al. (eds.): London: Academic
-
Bonné-Tamir B (1980) The Samaritans: A living ancient isolate. In AW Eriksson et al. (eds.): Population Structure and Genetic Disorders. London: Academic, pp 27-41.
-
(1980)
Population Structure and Genetic Disorders
, pp. 27-41
-
-
Bonné-Tamir, B.1
-
10
-
-
0028262286
-
Genetic mapping of the gene for Usher syndrome: Linkage analysis in a large Samaritan kindred
-
Bonné-Tamir B, Korostishevsky M, Kalinsky H, Seroussi E, Beker R, Weiss S, and Godel V (1994) Genetic mapping of the gene for Usher syndrome: Linkage analysis in a large Samaritan kindred. Genomics 20:36-42.
-
(1994)
Genomics
, vol.20
, pp. 36-42
-
-
Bonné-Tamir, B.1
Korostishevsky, M.2
Kalinsky, H.3
Seroussi, E.4
Beker, R.5
Weiss, S.6
Godel, V.7
-
11
-
-
0021362719
-
Genetic evolution of the Samaritans
-
Cazes MH and Bonné-Tamir B (1984) Genetic evolution of the Samaritans. J. Biosoc. Sci. 76:177-187.
-
(1984)
J. Biosoc. Sci.
, vol.76
, pp. 177-187
-
-
Cazes, M.H.1
Bonné-Tamir, B.2
-
12
-
-
85192649973
-
The chromosomal localization and cloning of human genes involved in sensorineural non-syndromic recessive deafness
-
Bethesda, M.D. Abstract
-
Chaib H, Dodé C, Place C, Ayadi H, Loiselet J, Vincent C, and Petit C (1995) The chromosomal localization and cloning of human genes involved in sensorineural non-syndromic recessive deafness. Symposium on Molecular Biology of Hearing and Deafness, Bethesda, M.D. Abstract, p. 22.
-
(1995)
Symposium on Molecular Biology of Hearing and Deafness
, pp. 22
-
-
Chaib, H.1
Dodé, C.2
Place, C.3
Ayadi, H.4
Loiselet, J.5
Vincent, C.6
Petit, C.7
-
13
-
-
0002956094
-
The heterogeneity of Usher syndrome
-
Pub. 426. Amsterdam Excerpta Media Foundation
-
Davenport SLH and Omenn GS (1977) The heterogeneity of Usher syndrome. Pub. 426. Amsterdam Excerpta Media Foundation. International Congress Series. Abstract 275:87-88.
-
(1977)
International Congress Series. Abstract
, vol.275
, pp. 87-88
-
-
Davenport, S.L.H.1
Omenn, G.S.2
-
14
-
-
0028836920
-
A gene for cogenital, 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, and Asher JH Jr (1995) A gene for cogenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17. Nature Genet. 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
-
15
-
-
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, and Smith RJH (1995a) Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q. Hum. Mol. Genet. 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
-
16
-
-
0028862795
-
An autosomal recessive non-syndromic form of sensorineural hearing loss maps to 3pDFNB6
-
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, and Smith RJH (1995b) An autosomal recessive non-syndromic form of sensorineural hearing loss maps to 3pDFNB6. Genome Res. 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
-
17
-
-
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, and Petit C (1994a) A non-syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q. Nature Genet. 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
-
18
-
-
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, and Petit C (1994b) A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene. Hum. Mol. Genet. 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
-
19
-
-
0028837681
-
A human recessive neuro-sensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dh) locus
-
Jain, PK, Iukushima K, Deshmuk HD, Arabandi R, Thomas E, Kumar S, Lalwani AK, Ploplis B, Skarka H, Srisailpathy CRS, Wayne S, Zbar RIS, Verma IC, Smith RJH, Wilcox ER. A human recessive neuro-sensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dh) locus. Hum. Mol. Genet. 4:2391-2394.
-
Hum. Mol. Genet.
, vol.4
, pp. 2391-2394
-
-
Jain, P.K.1
Iukushima, K.2
Deshmuk, H.D.3
Arabandi, R.4
Thomas, E.5
Kumar, S.6
Lalwani, A.K.7
Ploplis, B.8
Skarka, H.9
Srisailpathy, C.R.S.10
Wayne, S.11
Ris, Z.12
Verma, I.C.13
Smith, R.J.H.14
Wilcox, E.R.15
-
20
-
-
0002910360
-
Probable location of Usher type I gene on chromosome 14q by linkage with D14S13 (MLJ14 probe)
-
Kaplan J, Gerber S, Bonneau D, Rozet JM, Briard ML, Dufler JL, Munnich A, and Frezal J (1991) Probable location of Usher type I gene on chromosome 14q by linkage with D14S13 (MLJ14 probe). Cytogenet. Cell Genet. 58:A27446.
-
(1991)
Cytogenet. Cell Genet.
, vol.58
-
-
Kaplan, J.1
Gerber, S.2
Bonneau, D.3
Rozet, J.M.4
Briard, M.L.5
Dufler, J.L.6
Munnich, A.7
Frezal, J.8
-
21
-
-
0025308736
-
Localization of Usher syndrome type II to chromosome Iq
-
Kimberling WJW, Weston MD, Moller C, Davenport SLH, Shugart YY, Priluck IA, Martini A, and Smith RJH (1990) Localization of Usher syndrome type II to chromosome Iq. Genomics 7:245-249.
-
(1990)
Genomics
, vol.7
, pp. 245-249
-
-
Kimberling, W.J.W.1
Weston, M.D.2
Moller, C.3
Davenport, S.L.H.4
Shugart, Y.Y.5
Priluck, I.A.6
Martini, A.7
Smith, R.J.H.8
-
22
-
-
0027058412
-
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
-
Kimberling WJ, Moller CG, Davenport S, Priluck IA, Beighton PH, Greenberg J, Reardon W, Weston MD, Kenyon JB, Grunkemeyer JA, Pieke Dahl S, Overbeck LD, Blackwood DJ, Brower AM, Hoover DM, Rowland P, and Smith RJH (1992) Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11. Genomics 74:988-994.
-
(1992)
Genomics
, vol.74
, pp. 988-994
-
-
Kimberling, W.J.1
Moller, C.G.2
Davenport, S.3
Priluck, I.A.4
Beighton, P.H.5
Greenberg, J.6
Reardon, W.7
Weston, M.D.8
Kenyon, J.B.9
Grunkemeyer, J.A.10
Pieke Dahl, S.11
Overbeck, L.D.12
Blackwood, D.J.13
Brower, A.M.14
Hoover, D.M.15
Rowland, P.16
Smith, R.J.H.17
-
23
-
-
85192650904
-
Haplotype analysis of DNA microsatellites tightly linked to the locus of Usher syndrome type I on chromosome 11q
-
Korostishevsky M, Kalinsky H, Seroussi E, Weiss S, Vainder M, Sheffield VC, and Bonné-Tamir B (1994) Haplotype analysis of DNA microsatellites tightly linked to the locus of Usher syndrome type I on chromosome 11q. Am. J. Hum. Genet. 55:A191.
-
(1994)
Am. J. Hum. Genet.
, vol.55
-
-
Korostishevsky, M.1
Kalinsky, H.2
Seroussi, E.3
Weiss, S.4
Vainder, M.5
Sheffield, V.C.6
Bonné-Tamir, B.7
-
24
-
-
85192653268
-
Evidence for a fourth locus responsible for Usher syndrome type I (USID)
-
Abstract
-
Larget-Piet D, Gerber S, Rozet JM, Bonneav D, Mathieu M, Der Klaustian V, Munnich A, and Kaplan J (1995) Evidence for a fourth locus responsible for Usher syndrome type I (USID). Am. J. Phys. Anthropol. 57:A325. Abstract.
-
(1995)
Am. J. Phys. Anthropol.
, vol.57
-
-
Larget-Piet, D.1
Gerber, S.2
Rozet, J.M.3
Bonneav, D.4
Mathieu, M.5
Der Klaustian, V.6
Munnich, A.7
Kaplan, J.8
-
25
-
-
0025323589
-
Mapping recessive ophthalmic diseases: Linkage for Usher syndrome type II to a DNa marker on chromosome 1q
-
Lewis RA, Otterud B, Stauffcr D, Lalouel JM, and Leppert M (1990) Mapping recessive ophthalmic diseases: Linkage for Usher syndrome type II to a DNA marker on chromosome 1q. Genomics 7:250-256.
-
(1990)
Genomics
, vol.7
, pp. 250-256
-
-
Lewis, R.A.1
Otterud, B.2
Stauffcr, D.3
Lalouel, J.M.4
Leppert, M.5
-
26
-
-
0027989564
-
The A. thaliana disease resistance gene RDS2 encodes a protein containing a nucleotide-binding site and leucine-rich repeats
-
Mindrinos M, Katagiri F, Yu GL, and Ausubel M (1994) The A. thaliana disease resistance gene RDS2 encodes a protein containing a nucleotide-binding site and leucine-rich repeats. Cell 78:1089-1099.
-
(1994)
Cell
, vol.78
, pp. 1089-1099
-
-
Mindrinos, M.1
Katagiri, F.2
Yu, G.L.3
Ausubel, M.4
-
27
-
-
0026477244
-
New gene in the homologous human 11q13-q14 and mouse 7F chromosomal regions
-
Ollendorff V, Szepetowski P, Mattei MG, Gaudray P, and Birnbaum D (1992) New gene in the homologous human 11q13-q14 and mouse 7F chromosomal regions. Mammalian Genome 2:195-200.
-
(1992)
Mammalian Genome
, vol.2
, pp. 195-200
-
-
Ollendorff, V.1
Szepetowski, P.2
Mattei, M.G.3
Gaudray, P.4
Birnbaum, D.5
-
29
-
-
0015792305
-
Reproduction and inbreeding among the Samaritans
-
Roberts DF and Bonné B (1973) Reproduction and inbreeding among the Samaritans. Soc. Biol. 20:64-70.
-
(1973)
Soc. Biol.
, vol.20
, pp. 64-70
-
-
Roberts, D.F.1
Bonné, B.2
-
31
-
-
0028836898
-
Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q
-
Sankila EM, Pakarinen L, Kaariainen H, Aittomaki K, Karjalainen S, Sistonen P, and de la Chapelle A (1995) Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q. Hum. Mol. Genet. 4:93-98.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 93-98
-
-
Sankila, E.M.1
Pakarinen, L.2
Kaariainen, H.3
Aittomaki, K.4
Karjalainen, S.5
Sistonen, P.6
De La Chapelle, A.7
-
32
-
-
1842365784
-
Haplotype analysis and physical mapping to determine the position of Usher syndrome type I (USHIB) among closely linked micro-satellites on chromosome 11q13.5
-
Oxford, UK. Abstract
-
Seroussi E, Korostishevsky M, Sheffield VC, Gerhard D, and Bonné-Tamir B (1994) Haplotype analysis and physical mapping to determine the position of Usher syndrome type I (USHIB) among closely linked micro-satellites on chromosome 11q13.5. The 4th Chromosome 11 Workshop. Oxford, UK. Abstract.
-
(1994)
The 4th Chromosome 11 Workshop
-
-
Seroussi, E.1
Korostishevsky, M.2
Sheffield, V.C.3
Gerhard, D.4
Bonné-Tamir, B.5
-
33
-
-
0027058291
-
Localization of two genes for Usher syndrome type I to chromosome 11
-
Smith RJH, Lee EC, Kimberling WJ, Daiger SP, Pelias MZ, Keats BJB, Jay M, Bird A, Reardon W, Guest M, Ayyagari R, and Hejtmancik JF (1992) Localization of two genes for Usher syndrome type I to chromosome 11. Genomics 14:995-1002.
-
(1992)
Genomics
, vol.14
, pp. 995-1002
-
-
Smith, R.J.H.1
Lee, E.C.2
Kimberling, W.J.3
Daiger, S.P.4
Pelias, M.Z.5
Keats, B.J.B.6
Jay, M.7
Bird, A.8
Reardon, W.9
Guest, M.10
Ayyagari, R.11
Hejtmancik, J.F.12
-
34
-
-
0028815440
-
Defective Myosin VIIA gene responsible for Usher syndrome type IB
-
Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, Waish J, Mburv P, Varela A, Levilliers J, Weston MD, Kelly PM, Kimberling WJ, Wagenaar M, Levi-Acobas F, Larget-Piet D, Munnich A, Steel KP, Brown SDM, and Petit C (1955) Defective Myosin VIIA gene responsible for Usher syndrome type IB. Nature 374:60-61.
-
(1955)
Nature
, vol.374
, pp. 60-61
-
-
Weil, D.1
Blanchard, S.2
Kaplan, J.3
Guilford, P.4
Gibson, F.5
Waish, J.6
Mburv, P.7
Varela, A.8
Levilliers, J.9
Weston, M.D.10
Kelly, P.M.11
Kimberling, W.J.12
Wagenaar, M.13
Levi-Acobas, F.14
Larget-Piet, D.15
Munnich, A.16
Kp, S.17
Brown, S.D.M.18
Petit, C.19
-
35
-
-
0027931646
-
The product of the tobacco mosaic virus resistance gene N: Similarity to toll and the interleukin-1 receptor
-
Whitman S, Dinesh-Kumra SP, Choi D, Hehl R, Corr C, and Baker B (1994) The product of the tobacco mosaic virus resistance gene N: Similarity to toll and the interleukin-1 receptor. Cell 78:1101-1115.
-
(1994)
Cell
, vol.78
, pp. 1101-1115
-
-
Whitman, S.1
Dinesh-Kumra, S.P.2
Choi, D.3
Hehl, R.4
Corr, C.5
Baker, B.6
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