Identification of a hot spot for microdeletions in patients with X- linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4 |
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Authors: | de Kok, YJ Vossenaar, ER Cremers, CW Dahl, N Laporte, J Hu, LJ Lacombe, D Fischel-Ghodsian, N Friedman, RA Parnes, LS Thorpe, P Bitner-Glindzicz, M Pander, HJ Heilbronner, H Graveline, J den Dunnen, JT Brunner, HG Ropers, HH Cremers, FP |
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Affiliation: | Department of Human Genetics, University Hospital Nijmegen, The Netherlands. |
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