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E M De Leenheer

Showing results (1-10 of 4) with videos related to

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The Annals of Otology, Rhinology, and Laryngology|September 18, 2001
The DFNA10 phenotypeE M De Leenheer, P L Huygen, S Wayne, et al.
Archives of Otolaryngology--Head & Neck Surgery|February 15, 2001
Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13)E M De Leenheer, H H Kunst, W T McGuirt, et al.
Human Mutation|April 24, 2001
Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness familiesZ H Shah, M Toompuu, T Hakkinen, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 15, 2001
Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCHS J Bom, E M De Leenheer, F X Lemaire, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
The Annals of Otology, Rhinology, and Laryngology|September 18, 2001
The DFNA10 phenotypeE M De Leenheer, P L Huygen, S Wayne, et al.
Archives of Otolaryngology--Head & Neck Surgery|February 15, 2001
Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13)E M De Leenheer, H H Kunst, W T McGuirt, et al.
Human Mutation|April 24, 2001
Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness familiesZ H Shah, M Toompuu, T Hakkinen, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 15, 2001
Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCHS J Bom, E M De Leenheer, F X Lemaire, et al.
Pageof 1