Common Leukemia- and Lymphoma-Associated Genetic Aberrations in Healthy Individuals
Song, Jianbo, Mercer, Danielle, Hu, Xiaofeng, Liu, Henry, Li, Marilyn M
Published in The Journal of molecular diagnostics : JMD (01.03.2011)
Published in The Journal of molecular diagnostics : JMD (01.03.2011)
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Journal Article
Intratumoral Translocation Positive Heterogeneity in Pediatric Alveolar Rhabdomyosarcoma Tumors Correlates to Patient Survival Prognosis
Gleditsch, Katrina, Peñas, Jorge, Mercer, Danielle, Umrigar, Ayesha, Briscoe, James, Stark, Matthew, Tsien, Fern, Hollenbach, Andrew D.
Published in Frontiers in cell and developmental biology (18.09.2020)
Published in Frontiers in cell and developmental biology (18.09.2020)
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Journal Article
Delayed diagnosis of a patient with Usher syndrome 1C in a Louisiana Acadian family highlights the necessity of timely genetic testing for the diagnosis and management of congenital hearing loss
Umrigar, Ayesha, Musso, Amanda, Mercer, Danielle, Hurley, Annette, Glausier, Cassondra, Bakeer, Mona, Marble, Michael, Hicks, Chindo, Tsien, Fern
Published in SAGE open medical case reports (2017)
Published in SAGE open medical case reports (2017)
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Journal Article
Cytogenetic and molecular characterization of complex three-way translocations in acute promyelocytic leukemia
Freeman, Christopher E, Mercer, Danielle D, Ye, Yi, Van Brunt, 3rd, John, Li, Marilyn M
Published in Beijing da xue xue bao. Journal of Peking University. Yi xue ban (18.08.2009)
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Published in Beijing da xue xue bao. Journal of Peking University. Yi xue ban (18.08.2009)
Journal Article
Leading on the edge: The nature of paramedic leadership at the front line of care
Mercer, Danielle, Haddon, Arlene, Loughlin, Catherine
Published in Health care management review (01.01.2018)
Published in Health care management review (01.01.2018)
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Journal Article
Ghosts in the Adoption: Uncovering Parents' Attachment and Coping History
Buckwalter, Karen Doyle, Reed, Debbie, Mercer, Danielle
Published in Families in society (01.07.2017)
Published in Families in society (01.07.2017)
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Journal Article
Characterization of a cryptic 3.3 Mb deletion in a patient with a “balanced t(15;22) translocation” using high density oligo array CGH and gene expression arrays
Li, Marilyn M., Nimmakayalu, Manjunath A., Mercer, Danielle, Andersson, Hans C., Emanuel, Beverly S.
Published in American journal of medical genetics. Part A (01.02.2008)
Published in American journal of medical genetics. Part A (01.02.2008)
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Journal Article
Delayed diagnosis of a patient with Usher syndrome 1C in a Louisiana Acadian family highlights the necessity of timely genetic testing for the diagnosis and management of congenital hearing loss
Umrigar, Ayesha, Musso, Amanda, Mercer, Danielle, Hurley, Annette, Glausier, Cassondra, Bakeer, Mona, Marble, Michael, Hicks, Chindo, Tsien, Fern
Published in SAGE open medical case reports (01.01.2017)
Published in SAGE open medical case reports (01.01.2017)
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Characterization of a cryptic 3.3 Mb deletion in a patient with a "balanced t(15;22) translocation" using high density oligo array CGH and gene expression arrays
Li, Marilyn M., Nimmakayalu, Manjunath A., Mercer, Danielle, Andersson, Hans C., Emanuel, Beverly S.
Published in American Journal of Medical Genetics Part A (01.02.2008)
Published in American Journal of Medical Genetics Part A (01.02.2008)
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Report