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Alison Millson

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Clinical Chemistry|July 16, 2005
Direct molecular haplotyping of the IVS-8 poly(TG) and polyT repeat tracts in the cystic fibrosis gene by melting curve analysis of hybridization probesAlison Millson, Genevieve Pont-Kingdon, Sam Page, et al.
The Journal of Molecular Diagnostics : JMD|February 19, 2013
Triplet repeat primed PCR simplifies testing for Huntington diseaseMohamed Jama, Alison Millson, Christine E Miller, et al.
The Journal of Molecular Diagnostics : JMD|July 23, 2004
Long-range (17.7 kb) allele-specific polymerase chain reaction method for direct haplotyping of R117H and IVS-8 mutations of the cystic fibrosis transmembrane regulator geneGenevieve Pont-Kingdon, Mohamed Jama, Christine Miller, et al.
European Journal of Medical Genetics|May 31, 2016
Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorderGifty Bhat, Danielle LaGrave, Alison Millson, et al.
Clinical Chemistry|April 12, 2008
Design and application of noncontinuously binding probes used for haplotyping and genotypingGenevieve Pont-Kingdon, Rebecca L Margraf, Kelli Sumner, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disabilityAlison Millson, Danielle Lagrave, Mary J H Willis, et al.
Genetic Testing and Molecular Biomarkers|August 24, 2012
Copy number variation and incomplete linkage disequilibrium interfere with the HCP5 genotyping assay for abacavir hypersensitivityRoberta Melis, Tracy Lewis, Alison Millson, et al.
American Journal of Medical Genetics. Part A|August 1, 2012
Medium chain acyl-CoA dehydrogenase deficiency detected among Hispanics by New Jersey newborn screeningSharon Anderson, Christina Botti, Bo Li, et al.
The Journal of Molecular Diagnostics : JMD|July 14, 2015
Processed Pseudogene Confounding Deletion/Duplication Assays for SMAD4Alison Millson, Tracey Lewis, Tina Pesaran, et al.
The Journal of Molecular Diagnostics : JMD|July 24, 2003
Comparison of two quantitative polymerase chain reaction methods for detecting HER2/neu amplificationAlison Millson, Arminda Suli, Leah Hartung, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Clinical Chemistry|July 16, 2005
Direct molecular haplotyping of the IVS-8 poly(TG) and polyT repeat tracts in the cystic fibrosis gene by melting curve analysis of hybridization probesAlison Millson, Genevieve Pont-Kingdon, Sam Page, et al.
The Journal of Molecular Diagnostics : JMD|February 19, 2013
Triplet repeat primed PCR simplifies testing for Huntington diseaseMohamed Jama, Alison Millson, Christine E Miller, et al.
The Journal of Molecular Diagnostics : JMD|July 23, 2004
Long-range (17.7 kb) allele-specific polymerase chain reaction method for direct haplotyping of R117H and IVS-8 mutations of the cystic fibrosis transmembrane regulator geneGenevieve Pont-Kingdon, Mohamed Jama, Christine Miller, et al.
European Journal of Medical Genetics|May 31, 2016
Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorderGifty Bhat, Danielle LaGrave, Alison Millson, et al.
Clinical Chemistry|April 12, 2008
Design and application of noncontinuously binding probes used for haplotyping and genotypingGenevieve Pont-Kingdon, Rebecca L Margraf, Kelli Sumner, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disabilityAlison Millson, Danielle Lagrave, Mary J H Willis, et al.
Genetic Testing and Molecular Biomarkers|August 24, 2012
Copy number variation and incomplete linkage disequilibrium interfere with the HCP5 genotyping assay for abacavir hypersensitivityRoberta Melis, Tracy Lewis, Alison Millson, et al.
American Journal of Medical Genetics. Part A|August 1, 2012
Medium chain acyl-CoA dehydrogenase deficiency detected among Hispanics by New Jersey newborn screeningSharon Anderson, Christina Botti, Bo Li, et al.
The Journal of Molecular Diagnostics : JMD|July 14, 2015
Processed Pseudogene Confounding Deletion/Duplication Assays for SMAD4Alison Millson, Tracey Lewis, Tina Pesaran, et al.
The Journal of Molecular Diagnostics : JMD|July 24, 2003
Comparison of two quantitative polymerase chain reaction methods for detecting HER2/neu amplificationAlison Millson, Arminda Suli, Leah Hartung, et al.
Pageof 2