• A FEMALE PATIENT WITH DUPLICATION OF 7p13-pter ASSOCIATED WITH DEL 20p13pter RESULTING FROM MALSEGREGATED PATERNAL 7;20 BALANCED TRANSLOCATION
• A malformed child with a recombinant chromosome 7, rec(7) dup p, derived from a maternal pericentric inversion inv(7)(p15q36)
• A marginal zone phenotype in follicular lymphoma with t(14;18) is associated with secondary cytogenetic aberrations typical of marginal zone lymphoma
• A patient with duplication (7)(p15.3p22.3) and deletion (7)(p22.3pter) characterized by array-CGH
• A report of pure 7p duplication syndrome and review of the literature
• Acute eosinophilic leukemia in a patient with preexistent myelodysplastic syndrome
• Borderline intelligence and discrete craniofacial dysmorphism in an adolescent female with partial trisomy 7p due to a de novo tandem duplication 7 (p15.1-->p21.3)
• Cardiac malformation of partial trisomy 7p/monosomy 18p and partial trisomy 18p/monosomy 7p in siblings as a result of reciprocal unbalanced malsegregation--and review of the literature
• Characterization of aneuploid populations with trisomy 7 and 20 derived from diploid human colonic epithelial cells
• Chromosomal analysis of Barrett's cells: demonstration of instability and detection of the metaplastic lineage involved
• Chromosomal Heterogeneity of the G-401 Rhabdoid Tumor Cell Line: Unusual Partial 7p Trisomy
• Chromosomal imbalance in the offspring of translocation carriers involving 7p. Further contribution with three cases to the partial trisomy 7p phenotype
• Chromosome 7 aberrations in a young girl with myelodysplasia and hepatoblastoma: an unusual association
• Chromosome 7 aneusomy in metaplastic breast carcinomas with chondroid, squamous, and spindle-cell differentiation
• Chromosome aberrations in renal tumors detected by fluorescence in situ hybridization
• Chromosome mis-segregation and cytokinesis failure in trisomic human cells
• Clinical and molecular characterization of a second case of 7p22.1 microduplication
• Cytogenetic and molecular analysis of an unbalanced translocation (X;7) (q28;p15) in a dysmorphic girl
• De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?
• Deletions of chromosome arms 7p and 7q in adult acute myeloid leukemia: a marker chromosome confirmed by array comparative genomic hybridization
• Discordant phenotypes in a mother and daughter with mosaic supernumerary ring chromosome 19 explained by a de novo 7q36.2 deletion and 7p22.1 duplication
• Epileptic crises associated with trisomy of the short arm of chromosome 7 (46,XY,7p+
• Estimation of aneuploidy for chromosomes 3, 7, 16, X and Y in spermatozoa from 10 normospermic men using fluorescence in-situ hybridization
• Evidence from skewed X inactivation for trisomy mosaicism in Silver-Russell syndrome
• Further delineation of 7p trisomy. Case report and review of literature
• Gene dosage analysis in Silver-Russell syndrome: use of quantitative competitive PCR and dual-color FISH to estimate the frequency of duplications in 7p11.2-p13
• Genetic profile of T-cell acute lymphoblastic leukemias with MYC translocations
• Germline and somatic abnormalities of chromosome 7 in Wilms' tumor
• Greater trochanteric stippling in trisomy 7p
• Hepatosplenic gammadelta T-cell lymphoma with ring chromosome 7, an isochromosome 7q equivalent clonal chromosomal aberration
• Interphase fluorescence in situ hybridization analysis detects a much higher rate of thyroid tumors with clonal cytogenetic deviations of the main cytogenetic subgroups than conventional cytogenetics
• Maternal serum positive triple test screening in a fetus with partial distal trisomy 7p associated with maternal 7p;18p translocation
• Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver-Russell syndrome
• Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature
• Partial 7p trisomy. Report of new phenotype features
• Partial trisomy 16q and partial monosomy 7p of a fetus derivated from paternal balanced translocation: A case report
• Partial trisomy 3p and monosomy 7p associated with tetralogy of Fallot and infantile seizure
• Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel
• Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family
• Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient
• Phenotype and micro-array characterization of duplication 11q22.1-q25 and review of the literature
• Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter
• Phenotypic findings due to trisomy 7p15.3-pter including the TWIST locus
• Phenotypic spectrum of interstitial 7p duplication in mosaic and non-mosaic forms
• Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly
• Prenatal diagnosis of a fetus with partial trisomy 7p
• Prenatal diagnosis of a rare case of 7q11.23 duplication syndrome
• 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
• Pure partial 7p trisomy including the TWIST, HOXA, and GLI3 genes
• Rare combination in an infant patient: trisomy 7p and tetralogy of Fallot
• Rare monosomy 7 and deletion 7p at diagnosis of chronic myeloid leukemia in accelerated phase
• Sequential numerical changes of chromosomes 7 and 18 in diffuse-type stomach cancer cell lines: combined comparative genomic hybridization, fluorescence in situ hybridization, and ploidy analyses
• Severe psychomotor retardation in a boy with a supernumerary derivative chromosome resulting in partial trisomy 21 and partial trisomy 7p
• Small duplication of chromosome (7)(p22.1p22.2) and consideration of a dup 7p syndrome critical region
• Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter)
• Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter)
• The cardiovascular abnormalities associated with duplicated segments of chromosome 7
• The parathyroid hormone-responsive B1 gene is interrupted by a t(1;7)(q42;p15) breakpoint associated with Wilms' tumour
• Trisomy 7p and malignant transformation of human breast epithelial cells following epidermal growth factor withdrawal
• Trisomy 7p resulting from 7p15;9p24 translocation: report of a new case and review of associated medical complications
• Trisomy 7p resulting from isochromosome formation and whole-arm translocation
• Trisomy 7p: association with several craniocerebral anomalies and spongy degeneration
• Trisomy 7p: report of 2 patients and literature review
• Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis