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A Parving

Showing results (121-130 of 132) with videos related to

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Scandinavian Audiology|January 1, 1997
Hearing in the elderly > or = 80 years of age. Prevalence of problems and sensitivityA Parving, M Biering-Sørenson, B Bech, et al.
Audiology : Official Organ of the International Society of Audiology|January 1, 1990
Hearing disorders in patients with insulin-dependent diabetes mellitusA Parving, C Elberling, V Balle, et al.
Scandinavian Audiology|January 1, 1997
Hearing instruments and health technology--an evaluationA Parving, M S Sørensen, K Carver, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|February 1, 1991
Evidence for diabetic encephalopathyA Dejgaard, A Gade, H Larsson, et al.
Ophthalmic Paediatrics and Genetics|September 1, 1990
The Yemenite deaf-blind hypopigmentation syndrome. A new oculo-dermato-auditory syndromeM Warburg, N Tommerup, S Vestermark, et al.
International Journal of Pediatric Otorhinolaryngology|October 19, 2004
Guidelines and recommendations for testing of Cx26 mutations and interpretation of resultsM Mazzoli, V Newton, A Murgia, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1977
Aniridia, cataract and gonadoblastoma in a mentally retarded girl with deletion of chromosome II. A clinicopathological case reportS R Andersen, P Geertinger, H W Larsen, et al.
Metabolic and Pediatric Ophthalmology|January 1, 1980
Aniridia and interstitial deletion of the short arm of chromosome 11M Warburg, M Mikkelsen, S R Andersen, et al.
Genomics|February 15, 1997
The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7qP Coucke, G Van Camp, O Demirhan, et al.
Human Molecular Genetics|June 9, 1998
Two frequent missense mutations in Pendred syndromeP Van Hauwe, L A Everett, P Coucke, et al.
Pageof 14

Showing results (121-130 of 132) with videos related to

Sort By:
Pageof 14
Scandinavian Audiology|January 1, 1997
Hearing in the elderly > or = 80 years of age. Prevalence of problems and sensitivityA Parving, M Biering-Sørenson, B Bech, et al.
Audiology : Official Organ of the International Society of Audiology|January 1, 1990
Hearing disorders in patients with insulin-dependent diabetes mellitusA Parving, C Elberling, V Balle, et al.
Scandinavian Audiology|January 1, 1997
Hearing instruments and health technology--an evaluationA Parving, M S Sørensen, K Carver, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|February 1, 1991
Evidence for diabetic encephalopathyA Dejgaard, A Gade, H Larsson, et al.
Ophthalmic Paediatrics and Genetics|September 1, 1990
The Yemenite deaf-blind hypopigmentation syndrome. A new oculo-dermato-auditory syndromeM Warburg, N Tommerup, S Vestermark, et al.
International Journal of Pediatric Otorhinolaryngology|October 19, 2004
Guidelines and recommendations for testing of Cx26 mutations and interpretation of resultsM Mazzoli, V Newton, A Murgia, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1977
Aniridia, cataract and gonadoblastoma in a mentally retarded girl with deletion of chromosome II. A clinicopathological case reportS R Andersen, P Geertinger, H W Larsen, et al.
Metabolic and Pediatric Ophthalmology|January 1, 1980
Aniridia and interstitial deletion of the short arm of chromosome 11M Warburg, M Mikkelsen, S R Andersen, et al.
Genomics|February 15, 1997
The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7qP Coucke, G Van Camp, O Demirhan, et al.
Human Molecular Genetics|June 9, 1998
Two frequent missense mutations in Pendred syndromeP Van Hauwe, L A Everett, P Coucke, et al.
Pageof 14