• Interstitial deletion of the long arm of chromosome 1, del(1)(q21 leads to q25) in a profoundly retarded 8-year-old girl with multiple anomalies
• Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization
• Molecular cytogenetic analysis of follicular lymphoma (FL) provides detailed characterization of chromosomal instability associated with the t(14;18)(q32;q21) positive and negative subsets and histologic progression
• Multiple craniofacial anomalies associated with an interstitial deletion of chromosome 1(q21->q25)
• Multiple craniofacial anomalies associated with an interstitial deletion of chromosome 1(q21->q25)
• Rearrangements of chromosome band 1p36 in non-Hodgkin's lymphoma
• Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21----q25) and del(1)(q41----q43)