Aimee S. Spikes

Chromosome 1p36 Deletions: The Clinical Phenotype and Molecular Characterization of a Common Newly Delineated Syndrome

Stuart K. Shapira, Christopher McCaskill, Hope Northrup et al. · The American Journal of Human Genetics · 1997 · 342 citations · Full text

Chromatin, Molecular Characterization, Gene Deletion Data +10

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE

Julia Parrish, Ben A. Oostra, Annemieke J.M.H. Verkerk et al. · Nature Genetics · 1994 · 205 citations · Full text

Fragile Site Distal, Cell Division, Natural Sciences +6

Diagnosis of CMT1A duplications and HNPP deletions by interphase FISH: Implications for testing in the cytogenetics laboratory

Lisa G. Shaffer, Gilbert M. Kennedy, Aimee S. Spikes et al. · American Journal of Medical Genetics · 1997 · 178 citations

Genetic Testing, Cytogenetics, Genetics +21

Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci

Sue Ann Berend, Aimee S. Spikes, Catherine D. Kashork et al. · American Journal of Medical Genetics · 2000 · 72 citations

DNA Rearrangements on Both Homologues of Chromosome 17 in a Mildly Delayed Individual with a Family History of Autosomal Dominant Carpal Tunnel Syndrome

Lorraine Potocki, Ken‐Shiung Chen, Thearith Koeuth et al. · The American Journal of Human Genetics · 1999 · 69 citations · Full text

Chromatin, Chromosome Dynamics, Mendelian Disorder +14