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Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafness. [electronic resource] by
- Vore, Abram P
- Chang, Eugene H
- Hoppe, Jane E
- Butler, Merlin G
- Forrester, Shawnia
- Schneider, Michael C
- Smith, Luke L H
- Burke, Daniel W
- Campbell, Colleen A
- Smith, Richard J H
Producer: 20060110
In:
Archives of otolaryngology--head & neck surgery vol. 131
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164.
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Identification of a Novel Frameshift Variant of [electronic resource] by
- Jang, Jeong Hun
- Oh, Jayoung
- Han, Jin Hee
- Park, Hye-Rim
- Kim, Bong Jik
- Lee, Sejoon
- Kim, Min Young
- Lee, Seungmin
- Oh, Doo-Yi
- Choung, Yun-Hoon
- Choi, Byung Yoon
Producer: 20190701
In:
Genetic testing and molecular biomarkers vol. 23
Availability: No items available.
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177.
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Retina-derived POU domain factor 1 coordinates expression of genes relevant to renal and neuronal development. [electronic resource] by
- Fiorino, Antonio
- Manenti, Giacomo
- Gamba, Beatrice
- Bucci, Gabriele
- De Cecco, Loris
- Sardella, Michele
- Buscemi, Giacomo
- Ciceri, Sara
- Radice, Maria T
- Radice, Paolo
- Perotti, Daniela
Producer: 20171120
In:
The international journal of biochemistry & cell biology vol. 78
Availability: No items available.
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