• A case of 7q distal trisomy syndrome associated with West syndrome
• A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)
• A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literature
• A molecular cytogenetic analysis of 7q31 in prostate cancer
• A new case of pure partial 7q duplication
• A rare case of hepatosplenic γδ T-cell lymphoma expressing CD19 with ring chromosome 7 and trisomy 8
• Anesthetic management of a boy with 7 q trisomy syndrome
• Application of fluorescent in situ hybridization in primary diagnosis of aplastic anemia by morphology
• Association of the shrinkage of uterine leiomyoma treated with GnRH agonist and deletion of long arm of chromosome 7
• Biclonal acute monoblastic leukemia showing del(7q) and trisomies 9 and 22
• Boy with seizures (West syndrome) and distal 7q duplication syndrome due to an unbalanced 7q;9p translocation
• Case report of rec(7)dup(7q)inv(7)(p22q22) and a review of the recombinants resulting from parental pericentric inversions on any chromosomes
• Central diabetes insipidus in a newborn with deletion of chromosome 7q
• Characterization of a de novo Supernumerary Neocentric Ring Chromosome Derived from Chromosome 7
• Characterization of a Wilms tumor in a 9-year-old girl with trisomy 18
• Chromosome 7 aberrations in a young girl with myelodysplasia and hepatoblastoma: an unusual association
• Chromosome 7 abnormalities in prostate cancer detected by dual-color fluorescence in situ hybridization
• Clinical and hematological characteristics of hepatosplenic T gamma/delta lymphoma with isochromosome for long arm of chromosome 7
• Clinical impact of the clone size in MDS cases with monosomy 7 or 7q deletion, trisomy 8, 20q deletion and loss of Y chromosome
• Clinical, cytogenetic, and molecular findings in a fetus with ultrasonic multiple malformations, 4q duplication, and 7q deletion: A case report and literature review
• Combined study of prostatic carcinoma by classical cytogenetic analysis and comparative genomic hybridization
• Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q
• Consistency of isochromosome 7q and trisomy 8 in hepatosplenic gammadelta T-cell lymphoma: detection by fluorescence In situ hybridization of a splenic touch-preparation from a pediatric patient
• Constitutional t(5;7)(q11;p15) rearranged to acquire monosomy 7q and trisomy 1q in a patient with myelodysplastic syndrome transforming to acute myelocytic leukemia
• Conventional and molecular cytogenetic features of myelodysplastic syndrome in China
• Cytogenetic analysis and clinical significance of chromosome 7 aberrations in acute leukaemia
• Cytogenetic and genetic pathways in therapy-related acute myeloid leukemia
• Cytogenetic findings in two new cases of hepatoblastoma
• De novo 7q deletion with a positive maternal serum triple test screening
• De novo dup(7)(q21q22.2) and cytogenetics of 7q21q34 duplications
• De novo duplication and deletions at 7q in a three-generation family
• Deletion 21q22.3 and duplication 7q35q36.3 in a Colombian girl: a case report
• Deletions of chromosome arms 7p and 7q in adult acute myeloid leukemia: a marker chromosome confirmed by array comparative genomic hybridization
• Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells
• Derivative (7)t(7;8)(q34;q21). a new additional cytogenetic abnormality in acute promyelocytic leukemia
• Detection of common chromosome abnormalities in myelodysplastic syndrome with a panel fluorescence in situ hybridization
• Direct chromosome analysis and FISH study of primary gastric cancer
• 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
• Duplication/deletion mosaicism of the 7q(21.1 --> 31.3) region
• Erythroblastic sarcoma presenting as bilateral ovarian masses in an infant with pure erythroid leukemia
• FISH and SNP-A karyotyping in myelodysplastic syndromes: improving cytogenetic detection of del(5q), monosomy 7, del(7q), trisomy 8 and del(20q)
• Frequent involvement of chromosomes 1, 3, 7 and 8 in splenic marginal zone B-cell lymphoma
• Genetic abnormalities and pathophysiology of MDS
• Hemophagocytic syndrome and hepatosplenic gammadelta T-cell lymphoma with isochromosome 7q and 8 trisomy
• Hepatosplenic gamma/delta T-cell lymphoma with isochromosome 7q, translocation t(7;21), and tetrasomy 8 in a 9-year-old girl
• Hepatosplenic gamma/delta T-cell lymphoma: a report of two cases in immunocompromised patients, associated with isochromosome 7q
• Hepatosplenic gammadelta T-cell lymphoma with ring chromosome 7, an isochromosome 7q equivalent clonal chromosomal aberration
• Hepatosplenic gammadelta-T-cell lymphoma with leukemic course after renal transplantation
• Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency
• Hypogammaglobulinemia and Silver-Russell phenotype associated with partial trisomy 7q and partial monosomy 21q
• Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report
• Implications of a Chr7q21.11 Microdeletion and the Role of the PCLO Gene in Developmental Delay
• Incidence and significance of cryptic chromosome aberrations detected by fluorescence in situ hybridization in acute myeloid leukemia with normal karyotype
• Intrauterine phenotype features of fetuses with 7q11.23 microduplication syndrome
• Isochromosome 7q and trisomy 8 are consistent primary, non-random chromosomal abnormalities associated with hepatosplenic T gamma/delta lymphoma
• Isochromosome 7q in adult Wilms' tumors: diagnostic and pathogenetic implications
• Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10
• Malignant peripheral nerve sheath tumor with rhabdomyoblastic differentiation (malignant triton tumor) with balanced t(7;9)(q11.2;p24) and unbalanced translocation der(16)t(1;16)(q23;q13)
• Many unbalanced translocations show duplication of a translocation participant. Clinical and cytogenetic implications in myeloid hematologic malignancies
• Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)pat
• Numerical chromosomal changes and risk of development of myelodysplastic syndrome--acute myeloid leukemia in patients with Fanconi anemia
• Partial monosomy 7q
• Partial trisomy 2q(2q37.3-->qter) and monosomy 7q(7q34--->qter) due to paternal reciprocal translocation 2;7: a case report
• Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findings
• Partial trisomy of 7q: case report and literature review
• Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patient
• Phenotypic and genetic analysis of a child with partial trisomy 7q
• Pre- and perinatal findings in partial trisomy 7q resulting from balanced parental translocations t(7;21) and t(4;7)
• Prenatal diagnosis of a partial trisomy 7q in two fetuses with bilateral ventriculomegaly
• Prenatal diagnosis of a recombinant chromosome 7 resulting in trisomy 7q11.22 --> qter
• Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia
• Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2p
• Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly
• Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 --> qter) and partial monosomy 6q(6q26 --> qter) by high-resolution array CGH
• Prognostic Factors of Hepatosplenic T-cell Lymphoma: Clinicopathologic Study of 28 Cases
• Prognostic relevance of mutations and copy number alterations assessed with targeted next generation sequencing in IDH mutant grade II glioma
• Pure partial trisomy 7q: two new patients and review
• Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes
• Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes
• Recombinant chromosome 7 in a mosaic 45,X/47,XXX patient
• Recurrent Abnormal Clones in Myelodysplastic Syndrome Marrow Originate from Cells at a Pluripotent Stem Level and Maintain Their Early Differentiation Potency
• Ring chromosome 7 with amplification of 7q sequences in a pediatric case of hepatosplenic T-cell lymphoma
• Risk evaluation of carriers with chromosome reciprocal translocation t(7;13)(q34;q13) and concomitant meiotic segregation analyzed by FISH on ejaculated spermatozoa
• Risk factors for evolution of acquired aplastic anemia into myelodysplastic syndrome and acute myeloid leukemia after immunosuppressive therapy in children
• 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
• Short sternum: feature of trisomy chromosome 7 and a new association?
• Small inherited terminal duplication of 7q with hydrocephalus, cleft palate, joint contractures, and severe hypotonia
• Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter)
• Splenic marginal zone lymphoma: characterization of 7q deletion and its value in diagnosis
• Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35-->qter: molecular cytogenetic analysis and clinical phenotype in two generations
• Syndrome of facial, oral, and digital anomalies due to 7q21.2-->q22.1 duplication
• t(7;12)(q36;p13) and t(7;12)(q32;p13)--translocations involving ETV6 in children 18 months of age or younger with myeloid disorders
• The molecular pathogenesis of the myelodysplastic syndromes
• Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism
• Trisomy 7-harbouring non-random duplication of the mutant MET allele in hereditary papillary renal carcinomas
• Trisomy 7p and malignant transformation of human breast epithelial cells following epidermal growth factor withdrawal
• 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
• Unbalanced translocation der(1;7)(q10;p10) defines a unique clinicopathological subgroup of myeloid neoplasms
• Unbalanced translocation der(7)t(7q;11q): a new recurrent aberration leading to partial monosomy 7q and trisomy 11q in acute myeloid leukemia
• Variable expression of phenotype in offspring with partial monosomy 7q and partial trisomy 8p in a family with a rcp (7;8)(134;p12) translocation