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Glia
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January 1, 1989
Glial processes, identified through their glial-specific 130 kD surface glycoprotein, are juxtaposed to sites of neurogenesis in the leech germinal plate
R N Cole, R J Morell, B Zipser
Genomics
|
November 4, 1998
Tectorin-beta (Tectb) maps to mouse chromosome 19
H J Kim, K Noben-Trauth, R J Morell
Genomics
|
February 9, 2000
A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25
R J Morell, K H Friderici, S Wei, et al.
Ear and Hearing
|
August 31, 2001
Audiologic aspects of the search for DFNA20: a gene causing late-onset, progressive, sensorineural hearing loss
J L Elfenbein, R A Fisher, S Wei, et al.
Journal of Medical Genetics
|
April 3, 2004
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6)
S A Mohiddin, Z M Ahmed, A J Griffith, et al.
American Journal of Human Genetics
|
July 21, 2000
Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT
A J Griffith, A A Chowdhry, K Kurima, et al.
Clinical Genetics
|
February 19, 2008
A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1
L M Peters, R A Fridell, E T Boger, et al.
American Journal of Human Genetics
|
June 9, 2001
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
Z M Ahmed, S Riazuddin, S L Bernstein, et al.
American Journal of Human Genetics
|
September 19, 2003
Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26)
M Zhu, T Yang, S Wei, et al.
The New England Journal of Medicine
|
November 20, 1998
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness
R J Morell, H J Kim, L J Hood, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
Glia
|
January 1, 1989
Glial processes, identified through their glial-specific 130 kD surface glycoprotein, are juxtaposed to sites of neurogenesis in the leech germinal plate
R N Cole, R J Morell, B Zipser
Genomics
|
November 4, 1998
Tectorin-beta (Tectb) maps to mouse chromosome 19
H J Kim, K Noben-Trauth, R J Morell
Genomics
|
February 9, 2000
A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25
R J Morell, K H Friderici, S Wei, et al.
Ear and Hearing
|
August 31, 2001
Audiologic aspects of the search for DFNA20: a gene causing late-onset, progressive, sensorineural hearing loss
J L Elfenbein, R A Fisher, S Wei, et al.
Journal of Medical Genetics
|
April 3, 2004
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6)
S A Mohiddin, Z M Ahmed, A J Griffith, et al.
American Journal of Human Genetics
|
July 21, 2000
Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT
A J Griffith, A A Chowdhry, K Kurima, et al.
Clinical Genetics
|
February 19, 2008
A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1
L M Peters, R A Fridell, E T Boger, et al.
American Journal of Human Genetics
|
June 9, 2001
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
Z M Ahmed, S Riazuddin, S L Bernstein, et al.
American Journal of Human Genetics
|
September 19, 2003
Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26)
M Zhu, T Yang, S Wei, et al.
The New England Journal of Medicine
|
November 20, 1998
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness
R J Morell, H J Kim, L J Hood, et al.
Page
of 2