• 'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations
• "Complete" trisomy 5p; de novo translocation t(2;5)(q36;p11) with isochromosome 5p. Case report and review of the literature
• 3.7 Mb tandem microduplication in chromosome 5p13.1-p13.2 associated with developmental delay, macrocephaly, obesity, and lymphedema. Further characterization of the dup(5p13) syndrome
• A coalescence of two syndromes in a girl with terminal deletion and inverted duplication of chromosome 5
• A de novo cryptic 5p deletion and 9p duplication detected by subtelomeric MLPA in a boy with cri du chat syndrome
• A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome
• A new case of "complete" trisomy 5p with isochromosome 5p associated with a de novo translocation t(5;8)(q11;p23)
• A new case of trisomy 5 as sole cytogenetic anomaly in acute myeloid leukemia
• A patient with an interstitial duplication of chromosome 5p11-p13.3 further confirming a critical region for 5p duplication syndrome
• A Small Supernumerary Marker Derived from the Pericentromeric Region of Chromosome 5: Case Report and Delineation of Partial Trisomy 5p Phenotype
• Apparent Opitz BBBG syndrome with a partial duplication of 5p
• Association of schizophrenia and partial trisomy of chromosome 5p. A case report
• Atypical Peters' anomaly associated with partial trisomy 5p
• Cerebellar and brainstem hypoplasia in a child with a partial monosomy for the short arm of chromosome 5 and partial trisomy for the short arm of chromosome 10
• Characterization of a de novo complex chromosomal rearrangement in a patient with cri-du-chat and trisomy 5p syndromes
• Chromosome-wide aneuploidy study of cultured circulating myeloid progenitor cells from workers occupationally exposed to formaldehyde
• Clinical and genetic analysis of a rare case with mosaic partial trisomy 5p syndrome
• Clinical and molecular genetic characterization of two siblings with trisomy 2p24.3-pter and monosomy 5p14.3-pter
• Clinical delineation of a patient with trisomy 1q32.qter and monosomy 5p resulting from a familial translocation 1;5
• Clinical phenotype and molecular analysis of a three-generation family with an interstitial deletion of the short arm of chromosome 5
• Combined partial trisomy 3p/monosomy 5p resulting in sonographic abnormalities
• Cri-du-Chat Syndrome Cytogenetically Cryptic Recombination Aneusomy of Chromosome 5: Implications in Recurrence Risk Estimation
• Cytogenetic and molecular genetic diagnosis of a neonate with partial 13q trisomy and partial 5p monosomy
• De novo complete trisomy 5p: clinical and neuroradiological findings
• De novo complete trisomy 5p: clinical report and FISH studies
• Duplication (5p13 leads to pter): prenatal diagnosis and review of the literature
• Familial distal monosomy 5p15.3-pter with trisomy 12q24.2-qter resulting in neurodevelopmental delay and dysmorphic features
• Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5 (p151q333)
• Familial partial trisomy 5p resulting from segregation of an insertional translocation
• Familial transmission of 5p13.2 duplication due to maternal der(X)ins(X;5)
• Gain of an isochromosome 5p: a new recurrent chromosome abnormality in acute monoblastic leukemia
• Gain of an isochromosome 5p: a rare recurrent abnormality in acute myeloid leukemia
• Improved identification for 5p deletion syndrome and partial trisomy 11q presented in a fetus by SNP array
• Inherited unbalanced reciprocal translocation with 3q duplication and 5p deletion in a foetus revealed by cell-free foetal DNA (cffDNA) testing: a case report
• Interstitial deletion 5p accompanied by dicentric ring formation of the deleted segment resulting in trisomy 5p13-cen
• Isochromosome 5p and related anomalies: a novel recurrent chromosome abnormality in myeloid disorders
• Larsen-like phenotype associated with partial trisomy 3p and monosomy 5p
• Miller-Dieker syndrome and trisomy 5p in a child carrying a derivative chromosome with a microdeletion in 17p13.3 telomeric to the LIS1 and the D17S379 loci
• Modification of CMT1 phenotypes by the independent coexisting neurogenetic disorders, McArdle disease and chromosome 5p trisomy
• Molecular studies of segmental aneusomy: FISHing for the atypical cry in del(5)(p15.3)
• Monosomy 5p and trisomy 12p in a boy with familial balanced translocation
• Myelodysplastic syndrome with isochromosome 5p and trisomy 8 after treatment of a multiple myeloma
• Oculoauriculovertebral spectrum phenotype caused by an unbalanced t(5;8)(p15.31;p23.1) rearrangement
• Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation
• Partial distal 5p trisomy resulting from paternal translocation (5;15)(p15.1;p13) in a boy with no mental retardation
• Partial monosomy 5p and partial trisomy 5q due to paternal pericentric inversion 5(p15.1q35.1)
• Partial monosomy 5p and partial trisomy 5q due to paternal pericentric inversion of chromosome 5
• Partial trisomy 3p and monosomy 5p diagnosed by spectral karyotyping (SKY)
• Partial trisomy 4q and monosomy 5p inherited from a maternal translocationt(4;5)(q33; p15) in three adverse pregnancies
• PARTIAL TRISOMY 5p12-q 11.2 RESULTING FROM A MARKER CHROMOSOME: A NEW CASE REPORT WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER
• Partial trisomy for short and long arm of chromosome no. 5: Two cases of two possible syndromes
• Partial trisomy for short arm of chromosome 5
• Partial trisomy of chromosome 5p
• Periventricular heterotopia associated with chromosome 5p anomalies
• Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques
• Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly
• Prenatal diagnosis of partial trisomy 14q (14q31.1-->qter) and partial monosomy 5p (5p13.2-->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations
• Prognostic impact of trisomies of chromosomes 10, 17, and 5 among children with acute lymphoblastic leukemia and high hyperdiploidy (> 50 chromosomes)
• Proximal 5p trisomy resulting from a marker chromosome implicates band 5p13 in 5p trisomy syndrome
• Proximal partial 5p trisomy resulting from a maternal (19;5) insertion
• Pseudo dicentric chromosome (5;21): a rare example of maternal germline mosaicism
• Pure partial trisomy of the short arm of chromosome 5
• Recombination aneusomy of chromosome 5 associated with multiple severe congenital malformations
• Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement
• Reverse type of cri du chat disease: 5 p trisomy
• Second meiotic nondisjunction of the rearranged chromosome in a familial reciprocal 5/13 translocation
• Simultaneous trisomy 9q3 and monosomy 5p in two children with der(5),t(5;9)(p15.1;q34.13): report of an extended family
• Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual face
• Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype
• Tertiary trisomy due to a reciprocal translocation of chromosomes 5 and 21 in a four-generation family
• Tetrasomy 5p mosaicism due to an extra i(5p) in a severely affected girl
• Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)]
• Trisomy 5p due to paternal translocation (4;5) (q35;p12)
• Trisomy 5p with bilateral congenital diaphragmatic hernia: a case report
• Trisomy 5p: a report of 2 cases
• Trisomy 5p. A case report and review
• Trisomy of 5p and marker chromosomes
• Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3 p13.3)
• Trisomy of the short arm of chromosome 5: autopsy data in a malformed newborn with inv dup (5) (p13.1----p15.3)
• Unbalanced translocation (3;5)(q26.1;p14): a clinical report
• Variability in a family with an insertion involving 5p