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Dissertation/ Thesis

'n Ondersoek na die problematiek van inligtinggeletterdheid by die gehoorgestremde persoon in Suid-Afrika (Afrikaans)

Please read the abstract in the section 00front of this document
Dissertation (MA (Library Science))--University of Pretoria, 2007.
Information Science
unrestricted

Externí odkaz: http://hdl.handle.net/2263/26256
http://upetd.up.ac.za/thesis/available/etd-07132006-160520/

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Dissertation/ Thesis

Input and interaction in deaf families

Autor: Bogaerde, Elizabeth Marie van den

Proefschrift Universiteit van Amsterdam.
Omslag vermeldt: :LOT, Netherlands Graduate School of Linguistics, Landelijk[e] Onderzoekschool Taalwetenschap, en: IFOTT. - Auteursnaam op omslag: Beppie van den Bogaerde. Met lit. opg. - Met samenvattin

Externí odkaz: http://dare.uva.nl/document/55947

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Dissertation/ Thesis

Maatskaplike werk met dowes in Suid-Afrika

Autor: Pienaar, Izak Jacobus

Summaries in Afrikaans and English
Text in Afrikaans
Die teoretiese doelstellings van die ondersoek behels die verkenning van sommige maatskaplike behoeftes van Dowes, asook die aard van maatskaplikewerk-hulpverlening aan Dowes in Suid-Af r

Externí odkaz: http://hdl.handle.net/10500/15776

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Hoorhulpmiddelen; historische ontwikkelingen en toekomstverwachtingen

Dit rapport naar de stand van zaken en toekomstige medisch-technologische ontwikkelingen vormt een onderdeel van de Volksgezondheid Toekomst Verkenning 2002 van het Rijksinstituut voor Volksgezondheid en Milieu. De luchtgeleidings-hoortoestellen, de

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dris___00893::b7b9c01c8122381ac2c3552e6db91769

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Pastoral care and counselling of families with deaf children : a Practical Theological model

Autor: Pretorius, Rineé

PhD (Pastoral Studies), North-West University, Potchefstroom Campus, 2017 The research done in preparation for this study illustrates that – although extensive research has been done worldwide on Deaf culture, sign language, mental health services

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1399::de8e5ae5c46c478badd8f1126399b620
https://orcid.org/0000-0002-9829-2376

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Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21)

Autor: S. Velde, Alice Krebsová, C.W.R.J. Cremers, André Reis, G. Duijnhoven, F. Cremers, Patrick L. M. Huygen, Henricus P. M. Kunst, Henri A. M. Marres

Publikováno v: Clinical Otolaryngology, 25, 45-54
Clinical Otolaryngology, 25, pp. 45-54

An autosomal dominant trait of progressive, non-syndromic, non-specific mid-frequency sensorineural hearing impairment was identified in a Dutch family. Many affected family members (n = 21) were identified, among whom seven out of nine relatives age

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fe9071d6cf97135a1219c7cb76cb0b5
https://doi.org/10.1046/j.1365-2273.2000.00327.x

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The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases : identification of a somatic mosaicism for a POU3F4 missense mutation

Autor: Kok, Y.J.M. de, Cremers, C.W.R.J., Ropers, H.H., Cremers, F.P.M.

Publikováno v: Human Mutation, 10, pp. 207-211
Human Mutation, 10, 3, pp. 207-211
Human Mutation, 10, 207-211

Contains fulltext : 25053___.PDF (Publisher’s version ) (Open Access)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4d1f67f43b40305cf1103d3eaf319c3e
https://hdl.handle.net/2066/25053

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Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4

Autor: J. Graveline, H. Heilbronner, Rick A. Friedman, J.T. den Dunnen, Lorne S. Parnes, P. Thorpe, F. P. M. Cremers, Erik R. Vossenaar, Ling Jia Hu, Niklas Dahl, H.H. Ropers, H.-J. Pander, Didier Lacombe, Cor W. R. J. Cremers, Y.J.M. de Kok, Han G. Brunner, M. Bitner-Glindzicz, Nathan Fischel-Ghodsian, Jocelyn Laporte

Publikováno v: Human Molecular Genetics, 5, 1229-1235
Human Molecular Genetics, 5, 9, pp. 1229-1235
Human Molecular Genetics
Human Molecular Genetics, 1996, 5 (9), pp.1229-1235. ⟨10.1093/hmg/5.9.1229⟩

Small mutations in the POU domain gene POU3F4 were recently shown to cause X-linked deafness type 3 (DFN3) in nine unrelated males. The POU3F4 gene was found to be located outside four of five deletions associated with DFN3. Two of these deletions we

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bd5e13e62dfba3cc710910af17d4bb8
https://hdl.handle.net/2066/24064

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