• 47,XX,UPD(7)mat,+r(7)pat/46,XX,UPD(7)mat mosaicism in a girl with Silver-Russell syndrome (SRS): possible exclusion of the putative SRS gene from a 7p13-q11 region
• A case of lenalidomide-dependent myelodysplastic syndrome
• A fourth case of ring chromosome 7
• A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7
• Analysis of Cytogenetic Characteristics and Clinical Prognosis in 236 Patients with Myelodysplastic Syndrome
• Bilateral Cleft Lip and Palate in Ring Chromosome 7 Syndrome: A Case Report and Review of Clinical Characteristics
• Blaschkolinear malformation syndrome in complex trisomy-7 mosaicism
• Chromosome 7 abnormalities in acute megakaryoblastic leukemia associated with Down syndrome
• Chromosome 7 abnormalities in children with Down syndrome and preleukemia
• Chromosome abnormalities in a referred population for suspected chromosomal aberrations: a report of 4117 cases
• Chromosome abnormalities in bone marrow of Fanconi anemia patients
• Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases
• Complex structural involvement of chromosome 7 in primary myelodysplastic syndromes determined by fluorescence in situ hybridization
• Cutaneous findings in ring chromosome 7 syndrome
• Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989
• Cytogenetic studies in 112 cases of untreated myelodysplastic syndromes
• Cytogenomic and phenotypic analysis in low-level monosomy 7 mosaicism with non-supernumerary ring chromosome 7
• Detection of monosomy 7 and trisomies 8 and 11 in myelodysplastic disorders by interphase fluorescent in situ hybridization. Comparison with acute non-lymphocytic leukemias
• Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting
• 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
• Donor cell-derived myelodysplastic syndrome with ring chromosome 7 after allogeneic hematopoietic stem cell transplant in 2 patients with lymphomas as primary disease
• Five SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin (SMARC) genes are dispersed in the human genome
• Fluorescence in situ hybridisation studies to characterise complete and partial monosomy 7 in myeloid disorders
• Fluorescence in situ hybridization analysis of minute marker chromosomes in leukemia with monosomy 7
• Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russell syndrome
• Melanoma associated with ring chromosome 7
• Minimally differentiated acute myeloid leukemia with ring/marker derived from chromosome 7 in a child with Down syndrome
• Molecular cytogenetic characterization of a de novo mosaic supernumerary ring chromosome 7: report of a new patient
• Monosomy 7 and absence of 12q amplification in two cases of spindle cell liposarcomas
• Multiple circumferential skin folds and other anomalies: a problem in syndrome delineation
• Multiple desmoplastic Spitz nevi with BRAF fusions in a patient with ring chromosome 7 syndrome
• Myelodysplastic syndrome with atypical eosinophilia in association with ring chromosome 7. A case report
• Refractory anaemia with ring sideroblasts and monosomy 7 in a 10-year-old child
• Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequences
• Ring/marker chromosome derived from chromosome 7 in childhood acute megakaryoblastic leukemia with monosomy 7
• Silver-Russell syndrome and ring chromosome 7
• Sole abnormalities of chromosome 7 in myeloid malignancies: spectrum, histopathologic correlates, and prognostic implications
• Spectrum of Myelodysplastic Syndrome in Patients Evaluated for Cytopenia(s). A Report from a Reference Centre in Saudi Arabia
• The relationship between the myelodysplastic syndromes and the myeloproliferative disorders
• Williams-Beuren syndrome: phenotypic variability and deletions of chromosomes 7, 11, and 22 in a series of 52 patients