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Results: 1-3 |
Results: 3
Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13)
Authors: De Leenheer, EMR Kunst, HPM McGuirt, WT Prasad, SD Brown, MR Huygen, PLM Smith, RJH Cremers, WRJ
Citation: Emr. De Leenheer et al., Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13), ARCH OTOLAR, 127(1), 2001, pp. 13-17
The DFNA10 phenotype
Authors: De Leenheer, EMR Huygen, PLM Wayne, S Smith, RJH Cremers, WRJ
Citation: Emr. De Leenheer et al., The DFNA10 phenotype, ANN OTOL RH, 110(9), 2001, pp. 861-866
A family with autosomal dominant inherited dysmorphic small auricles, lip pits, and congenital conductive hearing impairment
Authors: Koch, SMP Kumar, S Cremers, WRJ
Citation: Smp. Koch et al., A family with autosomal dominant inherited dysmorphic small auricles, lip pits, and congenital conductive hearing impairment, ARCH OTOLAR, 126(5), 2000, pp. 639-644
Risultati: 1-3 |