Waardenburg syndrome von Read, A P, Newton, V E

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Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene von Tassabehji, Mayada, Newton, Valeria E., Read, Andrew P.

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Noise levels within the ear and post-nasal space in neonates in intensive care von Surenthiran, S S, Wilbraham, K, May, J, Chant, T, Emmerson, A J B, Newton, V E

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The mutational spectrum in Waardenburg syndrome von Tassabehji, Mayada, Newton, Valerie E., Liu, Xue-Zhong, Brady, Angela, Donnai, Dian, Krajewska-Walasek, Malgorzata, Murday, Victoria, Norman, Andrew, Obersztyn, Ewa, Reardon, William, Rice, John C., Trembath, Richard, Wieacker, Peter, Whiteford, Margo, Winter, Robin, Read, Andrew P.

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Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2 von Tassabehji, May, Read, Andrew P, Newton, Valerie E, Patton, Michael, Gruss, Peter, Harris, Rodney, Strachan, Tom

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PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse von Tassabehjl, M., Newton, V. E., Leverton, K., Turnbull, K., Seemanova, E., Kunze, J., Sperling, K., Strachan, T., Read, A. P.

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Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations — molecular and audiological findings von Mueller, R.F, Nehammer, A, Middleton, A, Houseman, M, Taylor, G.R, Bitner-Glindzciz, M, Van Camp, G, Parker, M, Young, I.D, Davis, A, Newton, V.E, Lench, N.J

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Evaluation of the use of a questionnaire to detect hearing loss in Kenyan pre-school children von Newton, Valerie E., Macharia, Isaac, Mugwe, Peter, Ototo, Benson, Kan, S.W.

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Waardenburg syndrome type II: Phenotypic findings and diagnostic criteria von Liu, Xue-Zhong, Newton, Valerie E., Read, Andrew P.

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Linkage Studies of Non-Syndromic Recessive Deafness (NSRD) in a Family Originating from the Mirpur Region of Pakistan Maps DFNB1 Centromeric to D13S175 von Brown, K. A., Janjua, A. H., Karbani, G., Parry, G., Noble, A., Crockford, G., Bishop, D. T., Newton, V. E., Markham, A. F., Mueller, R. F.

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Identification of a new mutation of the myosin VII head region in Usher syndrome type 1 von Liu, Xue-zhong, Newton, Valerie E., Steel, Karen P., Brown, Steve D. M.

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Hearing aids versus ventilation tubes in persistent otitis media with effusion: a survey of clinical practice von Ahmmed, A. U., Curley, J. W. A., Newton, V. E., Mukherjee, D.

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Symptomatic congenital cytomegalovirus infection after maternal recurrent infection von MORRIS, DAVID J, SIMS, DOUG, CHISWICK, MALCOLM, DAS, VIJAY K, NEWTON, VALERIE E

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Evaluation of the use of a questionnaire to detect hearing loss in babies in China von Newton, Valerie E., Liu, Xuezhong, Ke, Xiaomei, Xu, Lirong, Bamford, John M.

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Otoacoustic emissions in 28 young adults exposed to amplified music von Mansfield, J. D., Baghurst, P. A., Newton, V. E.

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Sensorineural hearing loss and the Marinesco-Sjögren syndrome von Newton, V. E.

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Genetic counselling for isolated hearing loss von Newton, V. E.

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Sound Localisation in Children with a Severe Unilateral Hearing Loss von Newton, V. E.

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Prescription of hearing aids for the elderly: The views of general practitioners von Newton, V. E., Hillier, V. F., Stephens, S. D. G.

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Hearing aid prescription in general practice von Newton, V E, Stephens, S D, Hillier, V F

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