• 46,XX,trcp(1;10),trcp(2;8) karyotype of maternal origin and 2p trisomy
• A case of complete trisomy 2p/triploidy mosaicism
• A case of partial trisomy 2p23-pter syndrome with trisomy 18p due to a de novo supernumerary marker chromosome
• A cryptic unbalanced translocation t(2;9)(p25.2;q34.3) causes the phenotype of 9q subtelomeric deletion syndrome and additional exophthalmos and joint contractures
• A familial inverted duplication/deletion of 2p25.1-25.3 provides new clues on the genesis of inverted duplications
• A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22
• A new entity in WHO classification of tumors of the central nervous system--embryonic tumor with abundant neuropil and true rosettes: case report and review of literature
• A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis
• A recurrent chondromyxoid fibroma with chromosome aberrations ins(5;2)(q13;p21p25) and 2p deletion: a case report
• A variant Burkitt-type translocation (2p-;8q+) in a patient with diffuse large cell lymphoma
• Agenesis of the lung associated with a chromosome abnormality (46,XX,2p+)
• Autosomal dominant congenital cataract and microphthalmia associated with a familial t(2;16) translocation
• Bilateral semilunar valve dysplasia in a patient with inverted duplication 2p25-22
• Characterization of a recurrent translocation t(2;3)(p15-22;q26) occurring in acute myeloid leukaemia
• Clinical and molecular genetic characterization of two siblings with trisomy 2p24.3-pter and monosomy 5p14.3-pter
• Cloning and characterization of human PREB; a gene that maps to a genomic region associated with trisomy 2p syndrome
• Confirmation of the prenatal mosaic trisomy 2 via fetal USG and cytogenetic analyses
• Congenital neuroblastoma in a patient with partial trisomy of 2p
• Constitutional 560.49 kb chromosome 2p24.3 duplication including the MYCN gene identified by SNP chromosome microarray analysis in a child with multiple congenital anomalies and bilateral Wilms tumor
• Cytogenetic and molecular characterization of a partial trisomy 2p arising from inverted duplication of 2p with terminal deletion of 2pter
• Description of a case of distal 2p trisomy by array-based comparative genomic hybridization: a high resolution genome-wide investigation for chromosomal aneuploidy in a single assay
• Distal trisomy 2p and arachnodactyly
• Duplication 2p and monosomy 8p in mosaicism: clinical, molecular cytogenetic and molecular markers of a unique case
• Duplication 2p25 in a child with clinical features of CHARGE syndrome
• Evolution of unbalanced gain of distal chromosome 2p in neuroblastoma
• Familial X-autosomal translocation t (X, 2)
• 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
• Germline duplication of chromosome 2p and neuroblastoma
• High resolution microarray CGH and MLPA analysis for improved genotype/phenotype evaluation of two childhood genetic disorder cases: ring chromosome 19 and partial duplication 2q
• Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency
• Holoprosencephaly: association with interstitial deletion of 2p and review of the cytogenetic literature
• Inflammatory arthropathies in children with chromosomal abnormalities
• Initial maternal meiotic I error leading to the formation of a maternal i(2q) and a paternal i(2p) in a healthy male
• Interstitial duplication of the short arm of chromosome 2: report of a new case and review
• Large Chromosome 2p Duplication-Associated Mechanisms and Clinical Presentations
• Metachronous neuroblastoma in an infant with germline translocation resulting in partial trisomy 2p: a role for ALK?
• Molecular cytogenetic studies in three patients with partial trisomy 2p, including CGH from paraffin-embedded tissue
• Neuroblastoma in a dysmorphic girl with a partial duplication of 2p caused by an unbalanced translocation
• Neuroblastoma in a pediatric patient with a microduplication of 2p involving the MYCN locus
• Paradoxical eyelid movement in trisomy 2p
• Parental balanced chromosomal rearrangement leading to major genomic imbalance and an autosomal trisomy resulting in consecutive pregnancy loss: a case report
• Partial monosomy 2p and partial trisomy 4q due to paternal translocation t(2;4)(p25.1;q31.3)
• Partial trisomy 2p
• Partial trisomy 2p and partial monosomy 2q arising from a paternal intrachromosomal 2q-into-2p between-arm insertion and paracentric inversion: molecular cytogenetic characterization of a four-break rearrangement
• Partial trisomy 2p24--&gt;pter and monosomy 18q22.1- qter resulting from parental translocation
• Partial trisomy of 2p and neuroblastoma
• Phenotype of a patient with pure partial trisomy 2p(p23--&gt;pter)
• Prenatal detection of cyclopia associated with interstitial deletion of 2p
• Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism
• 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
• Prenatal Diagnosis of Trisomy 2p due to Terminal 2p Duplication including Interstitial Telomeric Sequences
• Pure trisomy 2p syndrome in two siblings with an unbalanced translocation and minimal terminal 12q monosomy characterized by high-density microarray
• Recurrent inverted duplication of 2p with terminal deletion in a patient with the classical phenotype of trisomy 2p23-pter
• Regarding trisomy 2p syndrome
• Structural chromosomal mosaicism and prenatal diagnosis
• The 2p partial trisomy syndrome. Duplication of region 2p23 leads to 2pter in two members of a t(2;7) translocation kindred
• The chromosome 2 distal short arm trisomy syndrome
• The fetal phenotype in 2p trisomy
• Translocation of an immunoglobulin kappa locus to a region 3' of an unrearranged c-myc oncogene enhances c-myc transcription
• Trisomy 2p syndrome: a fetus with anencephaly and postaxial polydactyly
• Trisomy 2p: analysis of unusual phenotypic findings
• Unique case of trisomy 2p24.3-pter with no associated monosomy