Results
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281.
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282.
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283.
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284.
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Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia. [electronic resource] by
- Weil, D
- Levy, G
- Sahly, I
- Levi-Acobas, F
- Blanchard, S
- El-Amraoui, A
- Crozet, F
- Philippe, H
- Abitbol, M
- Petit, C
Producer: 19960618
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 93
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285.
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286.
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287.
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288.
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Clinical and genetic linkage analysis of a large Venezuelan kindred with Usher syndrome. [electronic resource] by
- Keogh, Ivan J
- Godinho, R N
- Wu, T Po
- Diaz de Palacios, A M
- Palacios, N
- Bello de Alford, M
- De Almada, M I
- MarPalacios, N
- Vazquez, A
- Mattei, R
- Seidman, C
- Seidman, J
- Eavey, R D
Producer: 20050531
In:
International journal of pediatric otorhinolaryngology vol. 68
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289.
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290.
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Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness. [electronic resource] by
- Ben Rebeh, Imen
- Morinière, Madeleine
- Ayadi, Leila
- Benzina, Zeineb
- Charfedine, Ilhem
- Feki, Jamel
- Ayadi, Hammadi
- Ghorbel, Abdelmonem
- Baklouti, Faouzi
- Masmoudi, Saber
Producer: 20110208
In:
Molecular vision vol. 16
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291.
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292.
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293.
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Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC. [electronic resource] by
- Ahmed, Zubair M
- Smith, Tenesha N
- Riazuddin, Saima
- Makishima, Tomoko
- Ghosh, Manju
- Bokhari, Sirosh
- Menon, Puthezhath S N
- Deshmukh, Dilip
- Griffith, Andrew J
- Riazuddin, Sheikh
- Friedman, Thomas B
- Wilcox, Edward R
Producer: 20020813
In:
Human genetics vol. 110
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294.
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295.
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Impact of the Usher syndrome on olfaction. [electronic resource] by
- Jansen, Fabian
- Kalbe, Benjamin
- Scholz, Paul
- Mikosz, Marta
- Wunderlich, Kirsten A
- Kurtenbach, Stefan
- Nagel-Wolfrum, Kerstin
- Wolfrum, Uwe
- Hatt, Hanns
- Osterloh, Sabrina
Producer: 20161213
In:
Human molecular genetics vol. 25
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296.
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297.
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298.
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299.
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Microarray-based mutation analysis of 183 Spanish families with Usher syndrome. [electronic resource] by
- Jaijo, Teresa
- Aller, Elena
- García-García, Gema
- Aparisi, María J
- Bernal, Sara
- Avila-Fernández, Almudena
- Barragán, Isabel
- Baiget, Montserrat
- Ayuso, Carmen
- Antiñolo, Guillermo
- Díaz-Llopis, Manuel
- Külm, Maigi
- Beneyto, Magdalena
- Nájera, Carmen
- Millán, Jose M
Producer: 20100326
In:
Investigative ophthalmology & visual science vol. 51
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300.
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Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children. [electronic resource] by
- Kimberling, William J
- Hildebrand, Michael S
- Shearer, A Eliot
- Jensen, Maren L
- Halder, Jennifer A
- Trzupek, Karmen
- Cohn, Edward S
- Weleber, Richard G
- Stone, Edwin M
- Smith, Richard J H
Producer: 20101130
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 12
Availability: No items available.
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