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Clinical Genetics
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May 29, 2008
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23
Z M Ahmed, S Riazuddin, S N Khan, et al.
Genomics
|
April 18, 1998
Chromosomal locations of three human nuclear genes (RPSM12, TUFM, and AFG3L1) specifying putative components of the mitochondrial gene expression apparatus
Z H Shah, V Migliosi, S C Miller, et al.
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.
Human Molecular Genetics
|
May 1, 1997
Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA)
R Morell, R A Spritz, L Ho, et al.
Advances in Oto-Rhino-Laryngology
|
June 27, 2000
DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15
T B Friedman, J T Hinnant, R A Fridell, et al.
Journal of Medical Genetics
|
May 1, 1995
Congenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese village
S Winata, I N Arhya, S Moeljopawiro, 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.
Genomics
|
March 2, 1999
A physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (del17p11.2p11.2)
F J Probst, K S Chen, Q Zhao, 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.
Nature Genetics
|
March 21, 1998
A mutation in PDS causes non-syndromic recessive deafness
X C Li, L A Everett, A K Lalwani, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 86) with videos related to
Sort By:
Page
of 9
Clinical Genetics
|
May 29, 2008
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23
Z M Ahmed, S Riazuddin, S N Khan, et al.
Genomics
|
April 18, 1998
Chromosomal locations of three human nuclear genes (RPSM12, TUFM, and AFG3L1) specifying putative components of the mitochondrial gene expression apparatus
Z H Shah, V Migliosi, S C Miller, et al.
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.
Human Molecular Genetics
|
May 1, 1997
Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA)
R Morell, R A Spritz, L Ho, et al.
Advances in Oto-Rhino-Laryngology
|
June 27, 2000
DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15
T B Friedman, J T Hinnant, R A Fridell, et al.
Journal of Medical Genetics
|
May 1, 1995
Congenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese village
S Winata, I N Arhya, S Moeljopawiro, 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.
Genomics
|
March 2, 1999
A physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (del17p11.2p11.2)
F J Probst, K S Chen, Q Zhao, 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.
Nature Genetics
|
March 21, 1998
A mutation in PDS causes non-syndromic recessive deafness
X C Li, L A Everett, A K Lalwani, et al.
Page
of 9