• A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter)
• A case of 3q21-qter trisomy and 3p25-pter monosomy syndrome
• A case of trisomy 22 in a live hereford calf
• A novel case of unilateral blepharophimosis syndrome and mental retardation associated with de novo trisomy for chromosome 3q
• A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24)
• A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24)
• Chromosome abnormalities in peripheral T-cell lymphoma
• Clinical and molecular cytogenetic analysis of a rare case of mosaicism for partial monosomy 3p and partial trisomy 10q in human
• Evidence for a 3p25 breakpoint hot spot region in thyroid tumors of follicular origin
• Fetal Cystic Hygroma Associated with Terminal 2p25.1 Duplication and Terminal 3p25.3 Deletion: Cytogenetic, Fluorescent <em>in Situ</em> Hybridization and Microarray Familial Characterization of Two Different Chromosomal Structural Rearrangeme
• Fetal Cystic Hygroma Associated with Terminal 2p25.1 Duplication and Terminal 3p25.3 Deletion: Cytogenetic, Fluorescent in Situ Hybridization and Microarray Familial Characterization of Two Different Chromosomal Structural Rearrangements
• Fluorescent In-situ Hybridization Study of Non-papillary Oncocytic/Eosinophilic Renal Cell Carcinoma
• Genomic Characterization of a Rare, de Novo Unbalanced ins(3;1)(p25.3;q21.3q23.3) in a Female Child with Multiple Congenital Anomalies
• Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defects
• Partial trisomy of the short arm of chromosome 3 (3p25 to 3pter). A distinct clinical entity
• Prenatal diagnosis of a fetus with 1p36 deletion syndrome and 3p26.3p25.2 duplication
• Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery
• Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes