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American Journal of Medical Genetics|April 15, 2000
Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II lociS A Berend, A S Spikes, C D Kashork, et al.
Cytogenetic and Genome Research|December 24, 2010
Visualization of fine-scale genomic structure by oligonucleotide-based high-resolution FISHN A Yamada, L S Rector, P Tsang, et al.
Genomics|April 28, 2000
Characterization of human retinal fascin gene (FSCN2) at 17q25: close physical linkage of fascin and cytoplasmic actin genesB E Tubb, S Bardien-Kruger, C D Kashork, et al.
Journal of Medical Genetics|June 14, 2000
Circadian rhythm abnormalities of melatonin in Smith-Magenis syndromeL Potocki, D Glaze, D X Tan, et al.
Nature Genetics|November 1, 1994
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXEJ E Parrish, B A Oostra, A J Verkerk, et al.
American Journal of Medical Genetics|November 11, 1996
Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11)C A Walter, L G Shaffer, C I Kaye, et al.
American Journal of Human Genetics|November 1, 1994
Molecular characterization of de novo secondary trisomy 13L G Shaffer, C McCaskill, J Y Han, et al.
American Journal of Medical Genetics|June 24, 1998
Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental originY Q Wu, V R Sutton, E Nickerson, et al.
The American Journal of Pathology|March 1, 1997
Allelic loss detected on chromosomes 8, 10, and 17 by fluorescence in situ hybridization using single-copy P1 probes on isolated nuclei from paraffin-embedded prostate tumorsD A Deubler, B J Williams, X L Zhu, et al.
American Journal of Human Genetics|October 27, 1997
Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndromeS K Shapira, C McCaskill, H Northrup, et al.
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