• 5G2 mutant mice model loss of a commonly deleted segment of chromosome 7q22 in myeloid malignancies
• A Case of Myelofibrosis and Myelodysplasia Identified Following Exposure to Isotretinoin
• A novel SAMD9 mutation causing MIRAGE syndrome: An expansion and review of phenotype, dysmorphology, and natural history
• A paediatric case of successful non-myeloablative bone marrow transplantation after azacitidine therapy for non-Down syndrome acute megakaryoblastic leukaemia with monosomy 7
• A Rare Case of ETV6/MECOM Rearrangement in Therapy-Related Acute Myeloid Leukemia with t(3;12) and Monosomy 7
• Acquisition of monosomy 7 and a RUNX1 mutation in Pearson syndrome
• Autism Spectrum Disorders: Analysis of Mobile Elements at 7q11.23 Williams-Beuren Region by Comparative Genomics
• Autoimmune Myelofibrosis in a 12-Year-old Male With Monosomy 7, Systemic Lupus Erythematous and Lupus Nephritis: A Case Report and Review of the Literature
• B-lymphocyte deficiency and recurrent respiratory infections in a 6-month-old female infant with mosaic monosomy 7
• Case Report: Refractory Cytopenia With a Switch From a Transient Monosomy 7 to a Disease-Ameliorating del(20q) in a <em>NHEJ1</em>-Deficient Long-term Survivor
• Clinical and molecular profiling of AML patients with chromosome 7 or 7q deletions in the context of <em>TP53</em> alterations and venetoclax treatment
• Clinical features and genetic analysis of two children with Williams-Beuren syndrome
• Clinical features and prognostic factors of advanced myelodysplastic syndromes in children
• Clonal chromosomal aberrations in Philadelphia negative cells such as monosomy 7 and trisomy 8 may persist for years with no impact on the long term outcome in patients with chronic myeloid leukemia
• COBL is a novel hotspot for IKZF1 deletions in childhood acute lymphoblastic leukemia
• Combined acute myeloid leukemia and panhypopituitarism
• Comment on: Acquired monosomy 7 myelodysplastic syndrome in a child with clinical features of dyskeratosis congenita and IMAGe association
• Constitutional <em>SAMD9L</em> mutations cause familial myelodysplastic syndrome and transient monosomy 7
• Cord Blood Transplantation in 2 Infants Presenting Monosomy 7 Clonal Hematopoiesis: SAMD9 / SAMD9L Germline Mutation
• CRISPR screening in human hematopoietic stem and progenitor cells reveals an enrichment for tumor suppressor genes within chromosome 7 commonly deleted regions
• Cytogenetic abnormalities predict survival after allogeneic hematopoietic stem cell transplantation for pediatric acute myeloid leukemia: a PDWP/EBMT study
• Deletion 7q21.2-q22.1 in a case with split hand-split foot malformation, sensorineural hearing loss and intellectual disability: Phenotype subtypes and the correlation with genotypes
• Development of nephrotic syndrome during immunosuppressive treatment for aplastic anaemia with monosomy 7 in a 16-year-old boy: A case report
• Diabetes insipidus and acute myeloid leukemia harboring monosomy 7: report of two cases and literature review
• Diagnostics and Prognostication of Myelodysplastic Syndromes
• Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay
• Disappearance of monosomy 7 in a patient with aplastic anemia after eltrombopag treatment
• Emerging phenotypes linked to variants in <em>SAMD9</em> and MIRAGE syndrome
• ETV6-ABL1 fusion combined with monosomy 7 in childhood B-precursor acute lymphoblastic leukemia
• Familial Monosomy 7 Syndrome Associated with Myelodysplasia
• Fanconi anemia proteins participate in a break-induced-replication-like pathway to counter replication stress
• Functional consequence and therapeutic targeting of cryptic ALK fusions in monosomy 7 acute myeloid leukemia
• Gastrointestinal: Intestinal Behçet's disease-like ulcers associated with myelodysplastic syndrome with monosomy 7
• Genetics of donor cell leukemia in acute myelogenous leukemia and myelodysplastic syndrome
• Germline predisposition in myeloid neoplasms: Unique genetic and clinical features of GATA2 deficiency and SAMD9/SAMD9L syndromes
• Germline SAMD9 and SAMD9L mutations are associated with extensive genetic evolution and diverse hematologic outcomes
• Greig Cephalopolysyndactyly Contiguous Gene Syndrome: Case Report and Literature Review
• Heterogeneity of GATA2-related myeloid neoplasms
• Identification of a cytogenetic and molecular subgroup of acute myeloid leukemias showing sensitivity to L-Asparaginase
• IKZF1 Deletions with COBL Breakpoints Are Not Driven by RAG-Mediated Recombination Events in Acute Lymphoblastic Leukemia
• Independent Prognostic Significance of Monosomy 17 and Impact of Karyotype Complexity in Monosomal Karyotype/Complex Karyotype Acute Myeloid Leukemia: Results from Four ECOG-ACRIN Prospective Therapeutic Trials
• Integrated genomic sequencing in myeloid blast crisis chronic myeloid leukemia (MBC-CML), identified potentially important findings in the context of leukemogenesis model
• L-asparaginase as an efficient salvage therapy for refractory acute myeloid leukemia with chromosome 7 abnormalities: a case series
• Machine Learning of Bone Marrow Histopathology Identifies Genetic and Clinical Determinants in Patients with MDS
• MECOM rearrangement involving the MYC locus: Two additional patients with the rare translocation, t(3;8)(q26.2;q24), and molecular review
• Molecular Characterization of IDH Wild-type Diffuse Astrocytomas: The Potential of cIMPACT-NOW Guidelines
• Molecular Genetics Testing
• Monosomy 7 in Pediatric Myelodysplastic Syndromes
• Monosomy 7: recent progress
• Monosomy 7/del (7q) in inherited bone marrow failure syndromes: A systematic review
• Monosomy 7/del(7q) cause sensitivity to inhibitors of nicotinamide phosphoribosyltransferase in acute myeloid leukemia
• Multiorgan failure with abnormal receptor metabolism in mice mimicking Samd9/9L syndromes
• Mutant Samd9l expression impairs hematopoiesis and induces bone marrow failure in mice
• Mutational Landscape and Gene Expression Patterns in Adult Acute Myeloid Leukemias with Monosomy 7 as a Sole Abnormality
• Myelodysplastic and myeloproliferative disorders of childhood
• Myelodysplastic syndrome presenting with central diabetes insipidus is associated with monosomy 7, visible or hidden: report of two cases and literature review
• Myeloid malignancies with 5q and 7q deletions are associated with extreme genomic complexity, biallelic TP53 variants, and very poor prognosis
• Noonan syndrome-associated myeloproliferative disorder with somatically acquired monosomy 7: impact on clinical decision making
• Of gains and losses: SAMD9/SAMD9L and monosomy 7 in myelodysplastic syndrome
• Pancytopenia, eosinophilia and coagulation disorders in a patient with T-acute lymphoblastic leukemia in prolonged remission
• Parallel deletion and duplication at 7q11.23 in a silent carrier for two reciprocal syndromic disorders
• Parental origin of monosomy 7 in acute leukaemia
• Partial trisomy 16q and partial monosomy 7p of a fetus derivated from paternal balanced translocation: A case report
• PAX5, NOTCH3, CBFB, and ACD drive an activated RAS pathway and monosomy 7 to B-ALL and AML in donor cell leukemia
• Pediatric MDS and bone marrow failure-associated germline mutations in SAMD9 and SAMD9L impair multiple pathways in primary hematopoietic cells
• Pediatric Myelodysplastic Syndrome With Germline RRAS Mutation: Expanding the Phenotype of RASopathies
• Pediatric Pancytopenia and Monosomy 7: A Case Report of SAMD9L-Associated Disease
• Perturbed hematopoietic stem and progenitor cell hierarchy in myelodysplastic syndromes patients with monosomy 7 as the sole cytogenetic abnormality
• Prenatal diagnosis for a fetus with 5p deletion syndrome
• Prevalence of germline GATA2 and SAMD9/9L variants in paediatric haematological disorders with monosomy 7
• Prognostic significance of monosomal karyotype in myelodysplastic syndrome: a meta-analysis
• Prolonged Response in Patient With Multiply Relapsed B-cell Acute Lymphoblastic Leukemia and Monosomy-7 to Bortezomib, Lenalidomide, and Dexamethasone
• Puzzling pieces of chromosome 7 loss or deletion
• Rare monosomy 7 and deletion 7p at diagnosis of chronic myeloid leukemia in accelerated phase
• Reduction of Extramedullary Complications in Patients With Acute Myeloid Leukemia/Myelodysplastic Syndrome Treated With Azacitidine
• Response to trametinib of two pediatric myeloid malignancies cases harboring RAS mutation and monosomy 7
• Revertant somatic mosaicism as a cause of cancer
• Shallow whole-genome sequencing: a useful, easy to apply molecular technique for CNA detection on FFPE tumor tissue-a glioma-driven study
• Single cell T cell landscape and T cell receptor repertoire profiling of AML in context of PD-1 blockade therapy
• Single-cell dissection of monosomy 7 syndromes
• Single-cell RNA-seq reveals a distinct transcriptome signature of aneuploid hematopoietic cells
• Somatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation
• Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans
• Spectrum of Myelodysplastic Syndrome in Patients Evaluated for Cytopenia(s). A Report from a Reference Centre in Saudi Arabia
• Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome
• Spontaneous Remission of Monosomy 7 Six Years After Diagnosis
• Spontaneous resolution of refractory cytopenia of childhood with monosomy 7 in an infant without an identifiable genetic cause
• Successful controlled ovarian stimulation and vitrification of oocytes in an adolescent diagnosed with myelodysplastic/pre-malignant clone with monosomy 7
• Sustained remission with azacitidine monotherapy and an aberrant precursor B-lymphoblast population in juvenile myelomonocytic leukemia
• T-lymphoblastic lymphoma and acute myeloid leukaemia transformed from myeloid neoplasm with eosinophilia: a divergent evolution of myeloid neoplasm with monosomy 7 but no detectable tyrosine kinase gene rearrangements designated by the WHO Classification
• The der(1;7)(q10;p10) defining a distinct profile from -7/del(7q) in myelodysplastic syndromes: A systematic review and meta-analysis
• The enigma of monosomy 7
• The First Case of Adult Granular Acute Lymphoblastic Leukemia with <em>DNMT3A</em> Mutation and Monosomy 7
• The impact of concomitant cytogenetic abnormalities on acute myeloid leukemia with monosomy 7 or deletion 7q after HLA-matched allogeneic stem cell transplantation
• The significance of CUX1 and chromosome 7 in myeloid malignancies
• Therapeutic discovery for marrow failure with MDS predisposition using pluripotent stem cells
• Therapy-related myelodysplastic syndrome with monosomy 7 and metastatic renal cell carcinoma successfully treated with nivolumab: two birds with one stone
• Therapy-related Myeloid Neoplasms in Children: A Single-institute Study
• Two new cases of interstitial 7q35q36.1 deletion including CNTNAP2 and KMT2C
• Whole Exome Sequencing Identifies a Rare Mutation in NACAD as a Possible Cause of COVID Orchitis in Brothers