Medium chain acyl-CoA dehydrogenase deficiency detected among Hispanics by New Jersey newborn screening
Anderson, Sharon, Botti, Christina, Li, Bo, Millonig, James H., Lyon, Elaine, Millson, Alison, Karabin, Suzanne S.M., Brooks, Susan Sklower
Published in American journal of medical genetics. Part A (01.09.2012)
Published in American journal of medical genetics. Part A (01.09.2012)
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Journal Article
Direct Molecular Haplotyping of the IVS-8 Poly(TG) and PolyT Repeat Tracts in the Cystic Fibrosis Gene by Melting Curve Analysis of Hybridization Probes
Millson, Alison, Pont-Kingdon, Genevieve, Page, Sam, Lyon, Elaine
Published in Clinical chemistry (Baltimore, Md.) (01.09.2005)
Published in Clinical chemistry (Baltimore, Md.) (01.09.2005)
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Journal Article
Triplet Repeat Primed PCR Simplifies Testing for Huntington Disease
Jama, Mohamed, Millson, Alison, Miller, Christine E, Lyon, Elaine
Published in The Journal of molecular diagnostics : JMD (01.03.2013)
Published in The Journal of molecular diagnostics : JMD (01.03.2013)
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Journal Article
Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorder
Bhat, Gifty, LaGrave, Danielle, Millson, Alison, Herriges, John, Lamb, Allen N, Matalon, Reuben
Published in European journal of medical genetics (01.09.2016)
Published in European journal of medical genetics (01.09.2016)
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Journal Article
Processed Pseudogene Confounding Deletion/Duplication Assays for SMAD4
Millson, Alison, Lewis, Tracey, Pesaran, Tina, Salvador, David, Gillespie, Katrina, Gau, Chia-Ling, Pont-Kingdon, Genevieve, Lyon, Elaine, Bayrak-Toydemir, Pinar
Published in The Journal of molecular diagnostics : JMD (01.09.2015)
Published in The Journal of molecular diagnostics : JMD (01.09.2015)
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Journal Article
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 disability
Millson, Alison, LaGrave, Danielle, Willis, Mary J.H., Rowe, Leslie R., Lyon, Elaine, South, Sarah T.
Published in American journal of medical genetics. Part A (01.01.2012)
Published in American journal of medical genetics. Part A (01.01.2012)
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Journal Article
Copy number variation and incomplete linkage disequilibrium interfere with the HCP5 genotyping assay for abacavir hypersensitivity
Melis, Roberta, Lewis, Tracy, Millson, Alison, Lyon, Elaine, McMillin, Gwendolyn A, Slev, Patricia R, Swensen, Jeffrey
Published in Genetic testing and molecular biomarkers (01.09.2012)
Published in Genetic testing and molecular biomarkers (01.09.2012)
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Journal Article
Simultaneous Molecular Haplotyping of Both IVS8 (TG)^sub m^ and (T)^sub n^ Tracts in the CFTR Gene: Still a Challenge / Response to the letter "Simultaneous Molecular Haplotyping of Both IVS8 (TG)^sub m^ and (T)^sub n^ Tracts in the CFTR Gene: Still a Challenge" by Costa et al
Costa, Catherine, Goossens, Michel, Girodon, Emmanuelle, Millson, Alison
Published in Clinical chemistry (Baltimore, Md.) (01.08.2006)
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Published in Clinical chemistry (Baltimore, Md.) (01.08.2006)
Journal Article
Comparison of Two Quantitative Polymerase Chain Reaction Methods for Detecting HER2/ neu Amplification
Millson, Alison, Suli, Arminda, Hartung, Leah, Kunitake, Steve, Bennett, Ann, Nordberg, Mary C. Lowry, Hanna, Wedad, Wittwer, Carl T., Seth, Arun, Lyon, Elaine
Published in The Journal of molecular diagnostics : JMD (01.08.2003)
Published in The Journal of molecular diagnostics : JMD (01.08.2003)
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Journal Article
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 Gene
Pont-Kingdon, Genevieve, Jama, Mohamed, Miller, Christine, Millson, Alison, Lyon, Elaine
Published in The Journal of molecular diagnostics : JMD (01.08.2004)
Published in The Journal of molecular diagnostics : JMD (01.08.2004)
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Journal Article
Multicenter characterization and validation of the intron-8 poly(T) tract (IVS8-T) status in 25 Coriell cell repository cystic fibrosis reference cell lines for cystic fibrosis transmembrane conductance regulator (CFTR) gene mutation assays
Sebastian, Siby, Spitzer, Silvia G, Grosso, Leonard E, Amos, Jean, Schaefer, Frederick V, Lyon, Elaine, Wolff, Daynna J, Hajianpour, Atieh, Taylor, Annette K, Millson, Alison, Stenzel, Timothy T
Published in Clinical chemistry (Baltimore, Md.) (01.01.2004)
Published in Clinical chemistry (Baltimore, Md.) (01.01.2004)
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Journal Article
Simultaneous detection of C282Y and H63D hemochromatosis mutations by dual-color probes
Phillips, M, Meadows, C A, Huang, M Y, Millson, A, Lyon, E
Published in Molecular diagnosis (01.06.2000)
Published in Molecular diagnosis (01.06.2000)
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Journal Article
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 disability
Millson, Alison, LaGrave, Danielle, Willis, Mary J.H., Rowe, Leslie R., Lyon, Elaine, South, Sarah T.
Published in American Journal of Medical Genetics Part A (01.01.2012)
Published in American Journal of Medical Genetics Part A (01.01.2012)
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