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Archives of Pathology & Laboratory Medicine
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November 2, 2018
The Power of Proficiency Testing: Unraveling Single-Nucleotide Polymorphism Interference, With Potential Impact on Clinical Testing of Spinocerebellar Ataxia Type 3
Cristiane M Ida, Patrick A Lundquist, Karen Weck, et al.
Electrophoresis
|
June 24, 2004
Telomerase activity measurement in magnetically captured epithelial cells: comparison of slab-gel and capillary electrophoresis
Jennifer L Hess, Donald H Atha, Jing-fan Xu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 23, 2011
Hereditary hemochromatosis: laboratory evaluation
Thomas P Moyer, W Edward Highsmith, Thomas C Smyrk, et al.
Current Protocols in Human Genetics
|
April 23, 2008
Conversion Technology for the separation of maternal and paternal copies of any autosomal chromosome in somatic cell hybrids
W Edward Highsmith, Kevin J Meyer, Victoria M Marley, et al.
American Journal of Translational Research
|
December 4, 2009
Real time PCR detection of the PI*Z and PI*S mutations associated with alpha-1 antitrypsin deficiency
Claudine L Bartels, Angela L Marchetti, W Edward Highsmith, et al.
Ophthalmic Genetics
|
December 29, 2007
LOC387715/HTRA1 and complement factor H variants in patients with age-related macular degeneration seen at the mayo clinic
Jose S Pulido, Lisa M Peterson, Lejla Mutapcic, et al.
The Journal of Molecular Diagnostics : JMD
|
March 27, 2007
RET proto-oncogene genotyping using unlabeled probes, the masking technique, and amplicon high-resolution melting analysis
Rebecca L Margraf, Rong Mao, W Edward Highsmith, et al.
Clinical Chemistry
|
January 5, 2006
Mutation scanning of the RET protooncogene using high-resolution melting analysis
Rebecca L Margraf, Rong Mao, W Edward Highsmith, et al.
Ophthalmic Genetics
|
December 7, 2006
A splice-site mutation in CCM1/KRIT1 is associated with retinal and cerebral cavernous hemangioma
Anna S Kitzmann, Jose S Pulido, Matthew J Ferber, et al.
The Journal of Molecular Diagnostics : JMD
|
June 29, 2011
Development and clinical implementation of a combination deletion PCR and multiplex ligation-dependent probe amplification assay for detecting deletions involving the human α-globin gene cluster
Benjamin R Kipp, Samantha E Roellinger, Patrick A Lundquist, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 66) with videos related to
Sort By:
Page
of 7
Archives of Pathology & Laboratory Medicine
|
November 2, 2018
The Power of Proficiency Testing: Unraveling Single-Nucleotide Polymorphism Interference, With Potential Impact on Clinical Testing of Spinocerebellar Ataxia Type 3
Cristiane M Ida, Patrick A Lundquist, Karen Weck, et al.
Electrophoresis
|
June 24, 2004
Telomerase activity measurement in magnetically captured epithelial cells: comparison of slab-gel and capillary electrophoresis
Jennifer L Hess, Donald H Atha, Jing-fan Xu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 23, 2011
Hereditary hemochromatosis: laboratory evaluation
Thomas P Moyer, W Edward Highsmith, Thomas C Smyrk, et al.
Current Protocols in Human Genetics
|
April 23, 2008
Conversion Technology for the separation of maternal and paternal copies of any autosomal chromosome in somatic cell hybrids
W Edward Highsmith, Kevin J Meyer, Victoria M Marley, et al.
American Journal of Translational Research
|
December 4, 2009
Real time PCR detection of the PI*Z and PI*S mutations associated with alpha-1 antitrypsin deficiency
Claudine L Bartels, Angela L Marchetti, W Edward Highsmith, et al.
Ophthalmic Genetics
|
December 29, 2007
LOC387715/HTRA1 and complement factor H variants in patients with age-related macular degeneration seen at the mayo clinic
Jose S Pulido, Lisa M Peterson, Lejla Mutapcic, et al.
The Journal of Molecular Diagnostics : JMD
|
March 27, 2007
RET proto-oncogene genotyping using unlabeled probes, the masking technique, and amplicon high-resolution melting analysis
Rebecca L Margraf, Rong Mao, W Edward Highsmith, et al.
Clinical Chemistry
|
January 5, 2006
Mutation scanning of the RET protooncogene using high-resolution melting analysis
Rebecca L Margraf, Rong Mao, W Edward Highsmith, et al.
Ophthalmic Genetics
|
December 7, 2006
A splice-site mutation in CCM1/KRIT1 is associated with retinal and cerebral cavernous hemangioma
Anna S Kitzmann, Jose S Pulido, Matthew J Ferber, et al.
The Journal of Molecular Diagnostics : JMD
|
June 29, 2011
Development and clinical implementation of a combination deletion PCR and multiplex ligation-dependent probe amplification assay for detecting deletions involving the human α-globin gene cluster
Benjamin R Kipp, Samantha E Roellinger, Patrick A Lundquist, et al.
Page
of 7