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R F Mueller

Showing results (81-90 of 85) with videos related to

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Journal of Medical Genetics|January 16, 1998
A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22D A Campbell, D P McHale, K A Brown, et al.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
Journal of Medical Genetics|August 3, 2001
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairmentL Van Laer, P Coucke, R F Mueller, et al.
Nature Genetics|December 2, 1999
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.
Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.
Pageof 9

Showing results (81-90 of 85) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 85 results.
Journal of Medical Genetics|January 16, 1998
A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22D A Campbell, D P McHale, K A Brown, et al.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
Journal of Medical Genetics|August 3, 2001
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairmentL Van Laer, P Coucke, R F Mueller, et al.
Nature Genetics|December 2, 1999
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.
Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.
Pageof 9