-
1
-
-
0036791660
-
Are attempts to have impaired children justifiable?
-
Anstey KW. 2002. Are attempts to have impaired children justifiable? J Med Ethics 28:286-288.
-
(2002)
J Med Ethics
, vol.28
, pp. 286-288
-
-
Anstey, K.W.1
-
2
-
-
0033659214
-
Parental attitudes toward genetic testing for pediatric deafness
-
Brunger JW, Murray GS, O'Riordan M, Matthews AL, Smith RJ, Robin NH. 2000. Parental attitudes toward genetic testing for pediatric deafness. Am J Hum Genet 67:1621-1625.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1621-1625
-
-
Brunger, J.W.1
Murray, G.S.2
O'Riordan, M.3
Matthews, A.L.4
Smith, R.J.5
Robin, N.H.6
-
3
-
-
0037165262
-
A deletion involving the connexin 30 gene in nonsyndromic hearing impairment
-
del Castillo I, Villamar M, Moreno-Pelayo MA, del Castillo FJ, Alvarez A, Telleria D, Menendez I, Moreno F. 2002. A deletion involving the connexin 30 gene in nonsyndromic hearing impairment. New Engl J Med 346(4):243-249.
-
(2002)
New Engl J Med
, vol.346
, Issue.4
, pp. 243-249
-
-
Del Castillo, I.1
Villamar, M.2
Moreno-Pelayo, M.A.3
Del Castillo, F.J.4
Alvarez, A.5
Telleria, D.6
Menendez, I.7
Moreno, F.8
-
4
-
-
33750707289
-
Genetics evaluation guidelines for the etiologic diagnosis of congenital hearing loss
-
Genetic Evaluation of Congenital Hearing Loss Expert Panel. 2002. Genetics evaluation guidelines for the etiologic diagnosis of congenital hearing loss. Genet Med 4:162-171.
-
(2002)
Genet Med
, vol.4
, pp. 162-171
-
-
-
5
-
-
0026795505
-
Ethical and cultural considerations in research on hereditary deafness
-
Grundfast K, Rosen J. 1992. Ethical and cultural considerations in research on hereditary deafness. Otolaryngologic Clin N Am 25(5):973-978.
-
(1992)
Otolaryngologic Clin N Am
, vol.25
, Issue.5
, pp. 973-978
-
-
Grundfast, K.1
Rosen, J.2
-
6
-
-
0033834029
-
Position statement: Principles and guidelines for early hearing detection and intervention programs (2000)
-
Joint Committee on Infant Hearing. 2000. Position statement: Principles and guidelines for early hearing detection and intervention programs (2000). Am J Audiol 9:9-29.
-
(2000)
Am J Audiol
, vol.9
, pp. 9-29
-
-
-
7
-
-
0036654536
-
GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: A HuGE review
-
Kenneson A, Van Naarden BK, Boyle C. 2002. GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: A HuGE review. Genet Med 4:258-274.
-
(2002)
Genet Med
, vol.4
, pp. 258-274
-
-
Kenneson, A.1
Van Naarden, B.K.2
Boyle, C.3
-
8
-
-
0036792630
-
Deafness, culture, and choice
-
Levy N. 2002. Deafness, culture, and choice. J Med Ethics 28:284.
-
(2002)
J Med Ethics
, vol.28
, pp. 284
-
-
Levy, N.1
-
9
-
-
0043244866
-
Attitudes of the broader hearing, deaf, and hard-of-hearing community toward genetic testing for deafness
-
Martinez A, Linden J, Schimmenti LA, Palmer CGS. 2003. Attitudes of the broader hearing, deaf, and hard-of-hearing community toward genetic testing for deafness. Genet Med 5:106-112.
-
(2003)
Genet Med
, vol.5
, pp. 106-112
-
-
Martinez, A.1
Linden, J.2
Schimmenti, L.A.3
Palmer, C.G.S.4
-
10
-
-
0032231301
-
Attitudes of deaf adults toward genetic testing for hereditary deafness
-
Middleton A, Hewison J, Mueller RF. 1998. Attitudes of deaf adults toward genetic testing for hereditary deafness. Am J Hum Genet 63:1175-1180.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1175-1180
-
-
Middleton, A.1
Hewison, J.2
Mueller, R.F.3
-
11
-
-
0035321843
-
Prenatal diagnosis for inherited deafness - What is the potential demand?
-
Middleton A, Hewison J, Mueller RF. 2001. Prenatal diagnosis for inherited deafness - what is the potential demand? J Genet Counseling 10:121-131.
-
(2001)
J Genet Counseling
, vol.10
, pp. 121-131
-
-
Middleton, A.1
Hewison, J.2
Mueller, R.F.3
-
12
-
-
0002682049
-
A world of their own
-
March 31, 2002
-
Mundy L. 2002. A world of their own. The Washington Post Magazine, March 31, 2002:22-43.
-
(2002)
The Washington Post Magazine
, pp. 22-43
-
-
Mundy, L.1
-
13
-
-
0034609284
-
Relation between choice of partner and high frequency of connexin-26 deafness
-
Nance WE, Liu XZ, Pandya A. 2000. Relation between choice of partner and high frequency of connexin-26 deafness. Lancet 356:500-501.
-
(2000)
Lancet
, vol.356
, pp. 500-501
-
-
Nance, W.E.1
Liu, X.Z.2
Pandya, A.3
-
14
-
-
0005932969
-
Cultural aspects of deafness (the deaf community)
-
Israel J, editor. Washington DC: Gallaudet Research Institute, Genetic Services Center, Gallaudet University
-
Prezioso CT. 1995. Cultural aspects of deafness (the deaf community). In: Israel J, editor. An introduction to deafness: A manual for genetic counselors. Washington DC: Gallaudet Research Institute, Genetic Services Center, Gallaudet University, pp 133-145.
-
(1995)
An Introduction to Deafness: A Manual for Genetic Counselors
, pp. 133-145
-
-
Prezioso, C.T.1
-
15
-
-
0033671717
-
Dominant modifier DFNM1 suppresses recessive deafness DFNB26
-
Riazuddin S, Castelein CM, Ahmed ZM, Lalwani AK, Mastroianni MA, Naz S, Smith TN, Liburd NA, Friedman TB, Griffith AJ, Riazuddin S, Wilcox ER. 2000. Dominant modifier DFNM1 suppresses recessive deafness DFNB26. Nat Genet 26:431-434.
-
(2000)
Nat Genet
, vol.26
, pp. 431-434
-
-
Riazuddin, S.1
Castelein, C.M.2
Ahmed, Z.M.3
Lalwani, A.K.4
Mastroianni, M.A.5
Naz, S.6
Smith, T.N.7
Liburd, N.A.8
Friedman, T.B.9
Griffith, A.J.10
Riazuddin, S.11
Wilcox, E.R.12
-
16
-
-
0037026891
-
Deaf lesbians, "designer disability," and the future of medicine
-
Savulescu J. 2002. Deaf lesbians, "designer disability," and the future of medicine. Br Med J 325:771-773.
-
(2002)
Br Med J
, vol.325
, pp. 771-773
-
-
Savulescu, J.1
-
17
-
-
0036085178
-
Attitudes of deaf and hard of hearing subjects toward genetic testing and prenatal diagnosis of hearing loss
-
Stern SJ, Arnos KS, Murrelle L, Welch KO, Nance WE, Pandya A. 2002. Attitudes of deaf and hard of hearing subjects toward genetic testing and prenatal diagnosis of hearing loss. J Med Genet 39:449-453.
-
(2002)
J Med Genet
, vol.39
, pp. 449-453
-
-
Stern, S.J.1
Arnos, K.S.2
Murrelle, L.3
Welch, K.O.4
Nance, W.E.5
Pandya, A.6
-
18
-
-
0035968605
-
Advances in hereditary deafness
-
Tekin M, Arnos KS, Pandya A. 2001. Advances in hereditary deafness. Lancet 358:1082-1090.
-
(2001)
Lancet
, vol.358
, pp. 1082-1090
-
-
Tekin, M.1
Arnos, K.S.2
Pandya, A.3
|