Disease: Chromosome 3- trisomy 3p
- 3p partial trisomy and 13q partial monosomy with congenital malformations and psychomotor developmental delay
- A large Indian family with rearrangement of chromosome 4p16 and 3p26.3 and divergent clinical presentations
- A patient with a duplication of chromosome 3p (p24.1p26.2): a comparison with other partial 3p trisomies
- Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomes
- Characterization of a rare mosaic unbalanced translocation of t(3;12) in a patient with neurodevelopmental disorders
- De novo trisomy 20p characterized by array comparative genomic hybridization: report of a novel case and review of the literature
- 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
- Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype
- Nodal marginal zone B-cell lymphoma showing prominent plasma cell differentiation in the pleural effusion: a case report
- Partial trisomy 3p and monosomy 5p diagnosed by spectral karyotyping (SKY)
- Partial trisomy 3p and partial monosomy 11q associated with double outlet right ventricle and septum pellucidum et vergae: a case report
- Phenotypic and genetic analysis of a boy with 3p26.3-pter deletion and 7q31.33-qter duplication
- Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter)
- Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization
- Several Fusion Genes Identified in a Spermatic Cord Leiomyoma With Rearrangements of Chromosome Arms 3p and 21q
- Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes