-
4
-
-
0033037643
-
Clinical Studies of Families with Hearing Loss Attributable to Mutations in the Connexin 26 Gene (GJB2/DFNB1)
-
Cohn, E. S., P. M. Kelley, T. W. Fowler, M. P. Gorga, D. M. Lefkowitz, H. J. Kuehn, G. B. Schaefer, L. S. Gobar, F. J. Hanh, D. J. Harris, and W. J. Kimberling, 1999. Clinical Studies of Families with Hearing Loss Attributable to Mutations in the Connexin 26 Gene (GJB2/DFNB1). Pediatrics 103:546-50
-
(1999)
Pediatrics
, vol.103
, pp. 546-550
-
-
Cohn, E.S.1
Kelley, P.M.2
Fowler, T.W.3
Gorga, M.P.4
Lefkowitz, D.M.5
Kuehn, H.J.6
Schaefer, G.B.7
Gobar, L.S.8
Hanh, F.J.9
Harris, D.J.10
Kimberling, W.J.11
-
5
-
-
70449959984
-
Deaf Parents Could Choose to Have Deaf Children
-
September 21
-
Connor, S. 2000. Deaf Parents Could Choose to Have Deaf Children. Independent News, September 21
-
(2000)
Independent News
-
-
Connor, S.1
-
7
-
-
9844252338
-
Prelingual Deafness: High Prevalence of a 3odelG Mutation in the Connexin 26 gene
-
Denoyelle, F., D. Weil, M. A. Maw, S. A. Wilcox, N. J. Lench, D. R. Allen-Powell, A. H. Osborn, H-H. M. Dahl, A. Middleton, M. J. Houseman, C. Dode, S. Marlin, A. Boulila-ElGaied, M. Grati, H. Ayadi, S. BenArab, P. Bitoun, G. Lina-Granade, J. Godet, M. Mustapha, J. Loiselet, E. El-Zir, A. Aubois, A. Joannard, R. J. McKinlay Gardner, and C. Petit. 1997. Prelingual Deafness: High Prevalence of a 3odelG Mutation in the Connexin 26 gene. Human Molecular Genetics 6:2173-77
-
(1997)
Human Molecular Genetics
, vol.6
, pp. 2173-2177
-
-
Denoyelle, F.1
Weil, D.2
Maw, M.A.3
Wilcox, S.A.4
Lench, N.J.5
Allen-Powell, D.R.6
Osborn, A.H.7
M.Dahl, H.-H.8
Middleton, A.9
Houseman, M.J.10
Dode, C.11
Marlin, S.12
Boulila-ElGaied, A.13
Grati, M.14
Ayadi, H.15
BenArab, S.16
Bitoun, P.17
Lina-Granade, G.18
Godet, J.19
Mustapha, M.20
Loiselet, J.21
El-Zir, E.22
Aubois, A.23
Joannard, A.24
McKinlay Gardner, R.J.25
Petit, C.26
more..
-
8
-
-
0032492217
-
Connexin-26 Mutations in Sporadic and Inherited Sensorineural Deafness
-
Estivill, X., P. Fortina, S. Surrey, R. Rabionet, S. Melchionda, L. D'Agruma, E. Mansfield, E. Rappaport, N. Govea, M. Mila, L. Zehnte, and P. Gasparini. 1998. Connexin-26 Mutations in Sporadic and Inherited Sensorineural Deafness. Lancet 351:394-98
-
(1998)
Lancet
, vol.351
, pp. 394-398
-
-
Estivill, X.1
Fortina, P.2
Surrey, S.3
Rabionet, R.4
Melchionda, S.5
D'Agruma, L.6
Mansfield, E.7
Rappaport, E.8
Govea, N.9
Mila, M.10
Zehnte, L.11
Gasparini, P.12
-
9
-
-
70449993269
-
Marriages of the Deaf in America: An Inquiry Covering the Results of Marriages of the Deaf in America
-
Washington, D.C
-
Fay, E. A. 1898. Marriages of the Deaf in America: An Inquiry Covering the Results of Marriages of the Deaf in America. Volta Bureau, Washington, D.C
-
(1898)
Volta Bureau
-
-
Fay, E.A.1
-
13
-
-
0031007349
-
Connexin 26 Mutations in Hereditary Non-Syndromic Sensorineural Deafness
-
Kelsell, D. P., J. Dunlop, H. P. Stevens, N. J. Lench, J. N. Liang, G. Parry, R. F. Mueller, and I. M. Leight. 1997. Connexin 26 Mutations in Hereditary Non-Syndromic Sensorineural Deafness. Nature 387:80-83
-
(1997)
Nature
, vol.387
, pp. 80-83
-
-
Kelsell, D.P.1
Dunlop, J.2
Stevens, H.P.3
Lench, N.J.4
Liang, J.N.5
Parry, G.6
Mueller, R.F.7
Leight, I.M.8
-
16
-
-
0027180952
-
Genetic Epidemiological Studies of Early-Onset Deafness in the U.S. School-Age Population
-
Marazita, M. L., L. M. Ploughman, B. Rawlings, E. Remington, K. S. Arnos, and W. E. Nance. 1993. Genetic Epidemiological Studies of Early-Onset Deafness in the U.S. School-Age Population. American Journal of Medical Genetics 46: 286-491
-
(1993)
American Journal of Medical Genetics
, vol.46
, pp. 286-491
-
-
Marazita, M.L.1
Ploughman, L.M.2
Rawlings, B.3
Remington, E.4
Arnos, K.S.5
Nance, W.E.6
-
19
-
-
3643059295
-
Mutations in the Connexin 26 Gene (GJB2) among Ashkenazi Jews with Nonsyndromic Recessive Deafness
-
Morrell, R. J., H. J. Kim, L. J. Hood, L. Goforth, K. Friderici, R. Risher, G. Van Camp, C. I. Berlin, C. Oddoux, H. Ostrer, B. Keats, and T. B. Friedman. 1998. Mutations in the Connexin 26 Gene (GJB2) among Ashkenazi Jews with Nonsyndromic Recessive Deafness. The New England Journal of Medicine 339:1500-05
-
(1998)
The New England Journal of Medicine
, vol.339
, pp. 1500-1505
-
-
Morrell, R.J.1
Kim, H.J.2
Hood, L.J.3
Goforth, L.4
Friderici, K.5
Risher, R.6
Van Camp, G.7
Berlin, C.I.8
Oddoux, C.9
Ostrer, H.10
Keats, B.11
Friedman, T.B.12
-
20
-
-
85122272636
-
Parables
-
ed. D. M. Bartels, B. S. Leroy, and A. L. Caplan, New York: Aldine de Gruyter
-
Nance, W. E. 1993. Parables. In Prescribing Our Future: Ethical Challenges in Genetic Counseling, ed. D. M. Bartels, B. S. Leroy, and A. L. Caplan, 89-94. New York: Aldine de Gruyter
-
(1993)
Prescribing Our Future: Ethical Challenges in Genetic Counseling
, pp. 89-94
-
-
Nance, W.E.1
-
21
-
-
0034531832
-
Statement of the American College of Medical Genetics on Universal Newborn Hearing Screening
-
Nance, W. E., G. C. Cunningham, J. G. Davis, C. C. Morton, L. J. Elsas, T. Finitzo, R. E. Falk, P. S. Ing, A. Pandya, E. R. B. McCabe, and R. J. H. Smith. 2000. Statement of the American College of Medical Genetics on Universal Newborn Hearing Screening. Genetics in Medicine 2:149-50
-
(2000)
Genetics in Medicine
, vol.2
, pp. 149-150
-
-
Nance, W.E.1
Cunningham, G.C.2
Davis, J.G.3
Morton, C.C.4
Elsas, L.J.5
Finitzo, T.6
Falk, R.E.7
Ing, P.S.8
Pandya, A.9
McCabe, E.R.B.10
Smith, R.J.H.11
-
22
-
-
0034609284
-
Relation between Choice of Partner and High Frequency of Connexin-26 Deafness
-
Nance, W. E., X. Z. Liu, and A. Pandya. 2000. Relation between Choice of Partner and High Frequency of Connexin-26 Deafness. Lancet 356:500-1
-
(2000)
Lancet
, vol.356
, pp. 500-501
-
-
Nance, W.E.1
Liu, X.Z.2
Pandya, A.3
-
23
-
-
0002169330
-
Genetic Analysis of Childhood Deafness
-
ed. F. Bess, New York: Grune and Stratton
-
Rose, S. P., P. M. Conneally, and W. E. Nance. 1977. Genetic Analysis of Childhood Deafness. In Childhood Deafness, ed. F. Bess, 19-35. New York: Grune and Stratton
-
(1977)
Childhood Deafness
, pp. 19-35
-
-
Rose, S.P.1
Conneally, P.M.2
Nance, W.E.3
-
25
-
-
0032547941
-
A New Era in the Genetics of Deafness
-
Steel, K. P. 1998. A New Era in the Genetics of Deafness. The New England Journal of Medicine. 339:1545-47
-
(1998)
The New England Journal of Medicine
, vol.339
, pp. 1545-1547
-
-
Steel, K.P.1
-
26
-
-
0003401949
-
The Attitudes of Deaf and Hard of Hearing Individuals toward Genetic Testing of Hearing Loss
-
Stern, S. J., K. Oelrich, K. S. Arnos, L. Murrelle, W. E. Nance, and A. Pandya. 2000. The Attitudes of Deaf and Hard of Hearing Individuals toward Genetic Testing of Hearing Loss. American Journal of Human Genetics 67(4), Suppl. 2:32
-
(2000)
American Journal of Human Genetics
, vol.67
, Issue.4 SUPPL. 2
, pp. 32
-
-
Stern, S.J.1
Oelrich, K.2
Arnos, K.S.3
Murrelle, L.4
Nance, W.E.5
Pandya, A.6
|