Aimee S. Spikes
Baylor College of Medicine(US)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Chromosomal and Genetic Variations, Prenatal Screening and Diagnostics, Hereditary Neurological Disorders, Congenital Heart Disease Studies
Most-Cited Works
- → Chromosome 1p36 Deletions: The Clinical Phenotype and Molecular Characterization of a Common Newly Delineated Syndrome(1997)342 cited
- → Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE(1994)205 cited
- → Diagnosis of CMT1A duplications and HNPP deletions by interphase FISH: Implications for testing in the cytogenetics laboratory(1997)178 cited
- → Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci(2000)72 cited
- → DNA Rearrangements on Both Homologues of Chromosome 17 in a Mildly Delayed Individual with a Family History of Autosomal Dominant Carpal Tunnel Syndrome(1999)69 cited
- → Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies(1995)25 cited
- → Trisomy 16q in a female newborn with a de novo X;16 translocation and hypoplastic left heart(1999)21 cited
- → Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings(1996)10 cited
- → Identification of Y chromatin directly in gonadal tissue by fluorescence in situ hybridization (FISH): Significance for Ullrich-Turner syndrome screening in the cytogenetics laboratory(2000)9 cited