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Author

Lai P. Nguyen

Observed name: Lai Nguyen
Institution: Mayo Clinic
Observed institution: Mayo Clinic
OpenAlex ID: A5036713192
Partial hexasomy for the Prader–Willi–Angelman syndrome critical region due to a maternally inherited large supernumerary marker chromosome
2010 · Nicole L. Hoppman‐Chaney, D. Brian Dawson, et al. · American Journal of Medical Genetics Part A · 43
Development of Five Dual-Color, Double-Fusion Fluorescence in Situ Hybridization Assays for the Detection of Common MLL Translocation Partners
2010 · Jeannette G. Keefe, William R. Sukov, et al. · Journal of Molecular Diagnostics · 11
Frequency, hematopathology, and detection of a new isodicentric variant of deletion 20q
2007 · Stephanie A. Smoley, Stephanie R. Fink, et al. · Cancer Genetics and Cytogenetics · 10
Whole Arm Duplication of 1q in Myeloid Neoplasm, with Emphasis On Derivative (1;7)(q10;p10).
2009 · Patricia T. Greipp, Curtis A Hanson, et al. · Blood · 1
Frequency, Hematopathology and Detection of a New Isodicentric Variant of Deletion 20q.
2006 · Stephanie R. Fink, Stephanie A. Smoley, et al. · Blood
Works count: 5
Citation count: 65
H-index: 3
I10-index: 3
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