Disease: Chromosome 13- partial monosomy 13q
- 11p15 duplication and 13q34 deletion with Beckwith-Wiedemann syndrome and factor VII deficiency
- 13q deletion is linked to an adverse phenotype and poor prognosis in prostate cancer
- 13q Deletion Syndrome Involving <em>RB1</em>: Characterization of a New Minimal Critical Region for Psychomotor Delay
- 13q interstitial deletion in a moroccan child with hereditary retinoblastoma and intellectual disability: A case report
- 13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijacking
- 13q13.3 microdeletion associated with apparently balanced translocation of 46,XX,t(7;13) suggests NBEA involvement
- 13q14 Deletion and Its Effect on Prognosis of Chronic Lymphocytic Leukemia
- 16p13.11 microdeletion in a patient with hemiconvulsion-hemiplegia-epilepsy syndrome: a case report
- 22.5 MB DELETION OF 13q31.1-q34 ASSOCIATED WITH HPE, DWM, AND HSCR: A CASE REPORT AND REDEFINING THE SMALLEST DELETED REGIONS
- A case of Feingold type 2 syndrome associated with keratoconus refines keratoconus type 7 locus on chromosome 13q
- A Case Study of Ring Chromosome 13 in a Pediatric Patient
- A de novo 13q31.3 microduplication encompassing the miR-17 ~ 92 cluster results in features mirroring those associated with Feingold syndrome 2
- A de novo 2.1-Mb deletion of 13q12.11 in a child with developmental delay and minor dysmorphic features
- A del(13)(q21.32q31.2)dn refined to 21.9 Mb in a female toddler with irides heterochromia and hypopigmentation: appraisal of interstitial mid-13q deletions
- A female patient with retinoblastoma and severe intellectual disability carrying an X;13 balanced translocation without rearrangement in the RB1 gene: a case report
- A higher percentage of cells with 13q deletion predicts worse outcome in Chinese patients with chronic lymphocytic leukemia carrying isolated 13q deletion
- A NEW OBSERVATION OF 13q DELETION SYNDROME: SEVERE UNDESCRIBED FEATURES
- A novel microdeletion involving the 13q31.3-q32.1 region in a patient with normal intelligence
- A Rare Co-occurrence of Intestinal Malrotation and Hirschsprung's Disease in a Neonate with 13q21.31q33.1 Interstitial Deletion Including the <em>EDNRB</em> Gene
- A rare unbalanced translocation (trisomy 5q33.3-qter, monosomy 13q34-qter) results in growth hormone deficiency and brain anomalies
- Acquired retinal pigmentary degeneration in a child with 13q deletion syndrome
- Acute Orbital Compromise after Intra-Arterial Chemotherapy in a Complex Retinoblastoma Associated with 13q Deletion Syndrome
- An acute myeloid leukemia case with concurrent 11q23 anomaly and D13S319 deficiency diagnosed by combined inter- and metaphase fluorescence in situ hybridization
- An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.3
- BCL2 and miR-15/16: from gene discovery to treatment
- Bilateral Cleft Lip and Palate Accompanied by 13q- Syndrome with Deficiencies of FVII and FX: A Case Report
- Blake's pouch cyst in 13q deletion syndrome: Posterior fossa malformations may occur due to disruption of multiple genes
- Case report: Concomitant Chronic Lymphocytic Leukaemia and Cytogenetically Normal de novo Acute Leukaemia in a Patient
- Characterization of CD34-deficient myofibroblastomas of the breast
- Chromosome 13 deletion and hypodiploidy on conventional cytogenetics are robust prognostic factors in Korean multiple myeloma patients: web-based multicenter registry study
- Chromosome 13q deletion syndrome involving 13q31‑qter: A case report
- Chromosome aberrations detected by conventional karyotyping using novel mitogens in chronic lymphocytic leukemia: Clinical and biologic correlations
- Clinical and genetic analysis of a child with chromosomal 13q32.1-q33.3 deletion
- Combining cytogenetic and epigenetic approaches in chronic lymphocytic leukemia improves prognosis prediction for patients with isolated 13q deletion
- Constitutive activation of NF-κB signaling by NOTCH1 mutations in chronic lymphocytic leukemia
- Conventional Cytogenetics and Interphase Fluorescence In Situ Hybridization Results in Multiple Myeloma: A Turkey Laboratory Analysis of 381 Cases
- Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India
- Cytogenetic Analysis of a Pseudoangiomatous Pleomorphic/Spindle Cell Lipoma
- Cytogenetic and molecular genetic diagnosis of a neonate with partial 13q trisomy and partial 5p monosomy
- Cytogenetics of Spindle Cell/Pleomorphic Lipomas: Karyotyping and FISH Analysis of 31 Tumors
- De Novo interstitial deletion 13q33.3q34 in a male patient with double outlet right ventricle, microcephaly, dysmorphic craniofacial findings, and motor and developmental delay
- Deletion of Chromosome 13 due to Different Rearrangements and Impact on Phenotype
- Dissecting chronic lymphocytic leukemia with 13q- using microRNA expression profile: Editorial for the paper "MiRNA expression profile of chronic lymphocytic leukemia patients with 13q deletion"
- Distal 13q monosomy and neural tube defects
- Early-Onset Diabetes Mellitus in a Patient With a Chromosome 13q34qter Microdeletion Including <em>IRS2</em>
- Effect of 13q deletion on IL-6 production in patients with multiple myeloma: a hypothesis may hold true
- EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorder
- Factor VII and factor X deficiency in a child with a chromosome 13q duplication and deletion
- First-line therapy for young patients with CLL
- Gene mutations connected to Waldenstöm macroglobulinemia
- Generation of a human induced pluripotent stem cells (MUi015-A) from skin fibroblast of retinoblastoma patient with 13q deletion syndrome
- Generation of induced pluripotent stem cells derived from primary and secondary myelofibrosis patient samples
- Genetic analysis of a child with 13q deletion syndrome featuring congenital heart disease
- Genetic testing in infantile spasms identifies a chromosome 13q deletion and retinoblastoma
- Genomic and Clinicopathologic Features of Primary Myelofibrosis With Isolated 13q Deletion
- Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34
- Influence of clone and deletion size on outcome in chronic lymphocytic leukemia patients with an isolated deletion 13q in a population-based analysis in British Columbia, Canada
- Interstitial 13q14 deletions detected in the karyotype and translocations with concomitant deletion at 13q14 in chronic lymphocytic leukemia: different genetic mechanisms but equivalent poorer clinical outcome
- Inversion duplication deletions involving the long arm of chromosome 13: phenotypic description of additional three fetuses and genotype-phenotype correlation
- Iris Hypoplasia as the Presenting Sign of Retinoblastoma in a Child With a 13q Deletion
- Jumping-like translocation-a rare chromosomal rearrangement in a patient with Burkitt lymphoma/leukemia
- Long-read genome sequencing resolves a complex 13q structural variant associated with syndromic anophthalmia
- Loss of a chromosomal region with synteny to human 13q14 occurs in mouse chronic lymphocytic leukemia that originates from early-generated B-1 B cells
- Magic mirror in my hand, which is the lineage in the end? A case of acute leukemia with hand-mirror cells
- miR-15a/16-1 deletion in activated B cells promotes plasma cell and mature B-cell neoplasms
- MiRNA expression profile of chronic lymphocytic leukemia patients with 13q deletion
- Molecular and cytogenetic evaluation of a patient with ring chromosome 13 and discordant results
- Molecular diagnosis in patients with retinoblastoma: Report of a series of cases
- Monosomy 13 in Mammary Myofibroblastoma
- Myofibroblastoma of the breast showing rare palisaded morphology and uncommon desmin- and CD34-negative immunophenotype: A case report
- Myofibroblastoma of the breast with smooth muscle differentiation showing deletion of 13q14 region: report of a case
- Novel case of paternal paracentric inversion causing partial trisomy 13 and review of the literature
- Novel recurrent chromosomal aberrations detected in clonal plasma cells of light chain amyloidosis patients show potential adverse prognostic effect: first results from a genome-wide copy number array analysis
- Onychomatricoma: a clinicopathological, immunohistochemical, and molecular study of 10 cases highlighting recurrent RB1 deletion and the potential diagnostic value of LEF-1
- Ophthalmological manifestations of 13q deletion syndrome: A case report
- Outcome of Patients with Multiple Myeloma and CKS1B Gene Amplification after Autologous Hematopoietic Stem Cell Transplantation
- Pan-cancer molecular analysis of the RB tumor suppressor pathway
- Partial trisomy 10p12.33 and partial monosomy 13q32.1: case report and a literature review
- Partial trisomy 10q (10q25.1 →qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization
- Partial Trisomy 13q/Monosomy 3p Resulting from a Paternal Reciprocal 3p;13q Translocation in a Boy with Facial Dysmorphism and Hypertrophic Cardiomyopathy
- PARTIAL TRISOMY 4p AND PARTIAL MONOSOMY 13q: CASE REPORT AND A LITERATURE REVIEW
- Partial Trisomy of Chromosome 13 with a Novel Translocation (8 ; 13) and Unique Clinical Presentation in a Palestinian Infant
- Patients with retinoblastoma and chromosome 13q deletions have increased chemotherapy-related toxicities
- Phenotypical characterization of 13q deletion syndrome: Report of two cases
- Postnatal diagnosis of constitutive ring chromosome 13 using both conventional and molecular cytogenetic approaches
- Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis
- Prenatal diagnosis of recurrent mosaic ring chromosome 13 of maternal origin
- Prenatal Sonographic Features of Rare Chromosome 13 Aberrations
- Prognostic Implications of Monosomies in Patients With Multiple Myeloma
- Quantitative PCR: an alternative approach to detect common copy number alterations in multiple myeloma
- Recurrent Sporadic Bilateral Retinoblastoma in a Child with 13q Deletion Syndrome
- Reduced anogenital distance, hematuria and left renal hypoplasia in a patient with 13q33.1-34 deletion: case report and literature review
- Retinoblastoma in Patients with 13q deletion syndrome - case series
- Retinoblastoma management in 13q deletion syndrome patients using super-selective chemotherapies and other cancer-directed interventions
- Risk stratification in multiple myeloma, part 2: the significance of genetic risk factors in the era of currently available therapies
- Solitary fibrous tumors: loss of chimeric protein expression and genomic instability mark dedifferentiation
- The clinical characteristics and prognosis of IGH deletion in multiple myeloma
- The morphology of CLL revisited: the clinical significance of prolymphocytes and correlations with prognostic/molecular markers in the LRF CLL4 trial
- The prognostic significance of 13q deletions of different sizes in patients with B-cell chronic lymphoproliferative disorders: a retrospective study
- Tourette syndrome, obsessive compulsive behavior, and dysmorphic features in a patient with deletions at chromosome 18q22.1 and chromosome 13q12.3-q13.1