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Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
January 7, 1998
X-inactivation and cytogenetic studies in a family with sensorineural hearing loss and Turner syndrome
N Sculerati, M A Perle, C Oddoux, et al.
The Laryngoscope
|
August 1, 1996
Hearing loss in Turner syndrome
N Sculerati, C Oddoux, C M Clayton, et al.
Applied Optics
|
June 12, 2010
Experimental evaluation of an unstable ring resonator with 90 degrees beam rotation: HiQ experimental results
S Holswade, R Riviere, C A Huguley, et al.
Nature Genetics
|
October 1, 1996
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
C Oddoux, J P Struewing, C M Clayton, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 22, 1999
Mendelian diseases among Roman Jews: implications for the origins of disease alleles
C Oddoux, E Guillen-Navarro, C Ditivoli, et al.
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of 2
Search research articles
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Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
January 7, 1998
X-inactivation and cytogenetic studies in a family with sensorineural hearing loss and Turner syndrome
N Sculerati, M A Perle, C Oddoux, et al.
The Laryngoscope
|
August 1, 1996
Hearing loss in Turner syndrome
N Sculerati, C Oddoux, C M Clayton, et al.
Applied Optics
|
June 12, 2010
Experimental evaluation of an unstable ring resonator with 90 degrees beam rotation: HiQ experimental results
S Holswade, R Riviere, C A Huguley, et al.
Nature Genetics
|
October 1, 1996
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
C Oddoux, J P Struewing, C M Clayton, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 22, 1999
Mendelian diseases among Roman Jews: implications for the origins of disease alleles
C Oddoux, E Guillen-Navarro, C Ditivoli, et al.
Page
of 2