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M Verstreken

Showing results (31-40 of 33) with videos related to

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Journal of Medical Genetics|May 19, 2001
A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutationE Fransen, M Verstreken, S J Bom, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Human Molecular Genetics|June 17, 1999
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.
Pageof 4

Showing results (31-40 of 33) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 33 results.
Journal of Medical Genetics|May 19, 2001
A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutationE Fransen, M Verstreken, S J Bom, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Human Molecular Genetics|June 17, 1999
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 familiesP J Coucke, P Van Hauwe, P M Kelley, et al.
Pageof 4