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Clinical Genetics
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June 24, 2011
High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in Israel
G Borck, L Rainshtein, S Hellman-Aharony, et al.
Nature Genetics
|
January 4, 2001
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
H Bolz, B von Brederlow, A Ramírez, et al.
Nature Genetics
|
June 30, 2001
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease
R C Betz, B G Schoser, D Kasper, et al.
Clinical Genetics
|
March 19, 2010
A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression
E Wilch, H Azaiez, R A Fisher, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 34) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 34 results.
Clinical Genetics
|
June 24, 2011
High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in Israel
G Borck, L Rainshtein, S Hellman-Aharony, et al.
Nature Genetics
|
January 4, 2001
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
H Bolz, B von Brederlow, A Ramírez, et al.
Nature Genetics
|
June 30, 2001
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease
R C Betz, B G Schoser, D Kasper, et al.
Clinical Genetics
|
March 19, 2010
A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression
E Wilch, H Azaiez, R A Fisher, et al.
Page
of 4