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Methods in Molecular Biology (Clifton, N.J.)
|
December 21, 2002
Multiplexed fluorescence analysis for mutations causing Tay-Sachs disease
Tracy L Stockley, Peter N Ray
American Journal of Medical Genetics. Part A
|
November 18, 2010
Novel duplication in glypican-4 as an apparent cause of Simpson-Golabi-Behmel syndrome
John Waterson, Tracy L Stockley, Summer Segal, et al.
Genetic Testing
|
January 27, 2007
Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophies
Tracy L Stockley, Sarah Akber, Natalie Bulgin, et al.
American Journal of Medical Genetics. Part A
|
December 6, 2011
CDKN1C mutations and genital anomalies
Holly I Welsh, Tracy L Stockley, Nicole Parkinson, et al.
The Laryngoscope
|
October 31, 2009
Pediatric cholesteatoma and variants in the gene encoding connexin 26
Adrian L James, Neil K Chadha, Blake C Papsin, et al.
American Journal of Medical Genetics. Part A
|
July 31, 2014
Paternal germline mosaicism for a GPC3 deletion in X-linked Simpson-Golabi-Behmel syndrome
Ron Agatep, Cheryl Shuman, Leslie Steele, et al.
International Journal of Pediatric Otorhinolaryngology
|
August 30, 2005
Ethnicity and mutations in GJB2 (connexin 26) and GJB6 (connexin 30) in a multi-cultural Canadian paediatric Cochlear Implant Program
Evan Jon Propst, Tracy L Stockley, Karen A Gordon, et al.
Genome Medicine
|
January 16, 2020
Molecular profiling for precision cancer therapies
Eoghan R Malone, Marc Oliva, Peter J B Sabatini, et al.
Journal of Clinical Pathology
|
May 31, 2020
Clinical implementation of circulating tumour DNA testing for <i>EGFR</i> T790M for detection of treatment resistance in non-small cell lung cancer
Tara Spence, Sheron Perera, Jessica Weiss, et al.
The Laryngoscope
|
February 10, 2006
Auditory responses in cochlear implant users with and without GJB2 deafness
Evan Jon Propst, Blake C Papsin, Tracy L Stockley, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 76) with videos related to
Sort By:
Page
of 8
Methods in Molecular Biology (Clifton, N.J.)
|
December 21, 2002
Multiplexed fluorescence analysis for mutations causing Tay-Sachs disease
Tracy L Stockley, Peter N Ray
American Journal of Medical Genetics. Part A
|
November 18, 2010
Novel duplication in glypican-4 as an apparent cause of Simpson-Golabi-Behmel syndrome
John Waterson, Tracy L Stockley, Summer Segal, et al.
Genetic Testing
|
January 27, 2007
Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophies
Tracy L Stockley, Sarah Akber, Natalie Bulgin, et al.
American Journal of Medical Genetics. Part A
|
December 6, 2011
CDKN1C mutations and genital anomalies
Holly I Welsh, Tracy L Stockley, Nicole Parkinson, et al.
The Laryngoscope
|
October 31, 2009
Pediatric cholesteatoma and variants in the gene encoding connexin 26
Adrian L James, Neil K Chadha, Blake C Papsin, et al.
American Journal of Medical Genetics. Part A
|
July 31, 2014
Paternal germline mosaicism for a GPC3 deletion in X-linked Simpson-Golabi-Behmel syndrome
Ron Agatep, Cheryl Shuman, Leslie Steele, et al.
International Journal of Pediatric Otorhinolaryngology
|
August 30, 2005
Ethnicity and mutations in GJB2 (connexin 26) and GJB6 (connexin 30) in a multi-cultural Canadian paediatric Cochlear Implant Program
Evan Jon Propst, Tracy L Stockley, Karen A Gordon, et al.
Genome Medicine
|
January 16, 2020
Molecular profiling for precision cancer therapies
Eoghan R Malone, Marc Oliva, Peter J B Sabatini, et al.
Journal of Clinical Pathology
|
May 31, 2020
Clinical implementation of circulating tumour DNA testing for <i>EGFR</i> T790M for detection of treatment resistance in non-small cell lung cancer
Tara Spence, Sheron Perera, Jessica Weiss, et al.
The Laryngoscope
|
February 10, 2006
Auditory responses in cochlear implant users with and without GJB2 deafness
Evan Jon Propst, Blake C Papsin, Tracy L Stockley, et al.
Page
of 8