• 14q deletions are associated with trisomy 12, NOTCH1 mutations and unmutated IGHV genes in chronic lymphocytic leukemia and small lymphocytic lymphoma
• 14q32.3-qter trisomic segment: a case report and literature review
• A 33-year-old male patient with paternal derived duplication of 14q11.2-14q22.1~22.3: clinical course, phenotypic and genotypic findings
• A case of CD5-positive mature B-cell neoplasm with t(10;14)(q24;q11.2) and trisomy 12
• A case of severe mental and developmental retardation associated with 14q terminal monosomy/5q terminal trisomy
• A case report of the neurocognitive and behavioral phenotype of mosaic trisomy 14
• 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 New Case of a Rare Combination of Temple Syndrome and Mosaic Trisomy 14 and a Literature Review
• A new case of partial 14q31.3-qter trisomy due to maternal pericentric inversion
• A new small supernumerary marker chromosome involving 14pter → q12 in a child with severe neurodevelopmental retardation: case report and literature review
• A novel dicentric chromosome, dic(9;9)(p12;q34), leading to trisomy 9 in follicular lymphoma without t(14;18)
• A severely short-statured girl with 47,XX, + 14/46,XX,upd(14)mat, mosaicism
• Acquired cystic disease-associated renal cell carcinoma: an immunohistochemical and fluorescence in situ hybridization study
• Acquisition of t(11;14) in a patient with chronic lymphocytic leukemia carrying both t(14;19)(q32;q13.1) and +12
• Acute myeloid leucaemia with trisomy 14 as a sole cytogenetic abnormality
• Azoospermia and trisomy 18p syndrome: a fortuitous association? A patient report and a review of the literature
• CASE-REPORT Low-level trisomy 14 mosaicism in a male newborn with ectrodactyly
• CD5 expression identifies a subset of splenic marginal zone lymphomas with higher lymphocytosis: a clinico-pathological, cytogenetic and molecular study of 24 cases
• Chromosomal imbalance in pigs showing a syndromic form of cleft palate
• Chromosomal microarray analysis allows prenatal detection of low level mosaic autosomal aneuploidy
• Chronic lymphocytic leukemia with a FGFR3 translocation: case report and literature review of an uncommon cytogenetic event
• Chronic lymphocytic leukemia with t(14 ;18) and trisomy 12: a case report
• Chronic lymphocytic leukemia with t(14;18)(q32;q21)
• Chronic lymphocytic leukemia with t(14;19)(q32;q13) is characterized by atypical morphologic and immunophenotypic features and distinctive genetic features
• Clinical and molecular findings in a patient with 46,XX/47,XX,+14 mosaicism caused by postzygotic duplication of a paternally derived chromosome 14
• Clinicopathologic Study of Chromosomal Aberrations in Ocular Adnexal Lymphomas of Korean Patients
• Clonal characteristics of acute lymphoblastic cells derived from BCR/ABL p190 transgenic mice
• Comparison of IGH Profile Signals Using t(4;14) and IGH Break-Apart Probes by FISH in Multiple Myeloma
• Complete trisomy 14 mosaicism: first live-born case in Korea
• Concurrent psu dic(21)(q22.3) and t(13;17)(q14.1;p12) in a mosaic Down's syndrome patient: review of thirty-one similar dicentrics
• Congenital ocular anomaly in an infant with trisomy 14 mosaicism
• Copy Number Variants Associated with 14 Cases of Self-Injurious Behavior
• Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India
• Cytogenetic analysis of 1572 cases of Down syndrome: a report of double aneuploidy and novel findings 47,XY, t(14;21)(q13;q22.3)mat,+21 and 45,XX,t(14;21) in an Indian population
• De Novo Duplication of Chromosome 9p in a Female Infant: Phenotype and Genotype Correlation
• Detection of copy number variants with chromosomal microarray in 10 377 pregnancies at a single laboratory
• Detection of genetic alterations in gastric cancer patients from Saudi Arabia using comparative genomic hybridization (CGH)
• Double Autosomal/Gonosomal Mosaic Trisomy 47,XXX/47,XX,+14 in a Newborn with Multiple Congenital Anomalies
• Enamel Pit Defects and Taurodontism in a Patient with Ring Chromosome 14 and 47,XXX
• Experience in prenatal ultrasound diagnosis of fetal microtia and associated abnormalities
• Familial small supernumerary marker chromosome (sSMC) (14)(:p11-q11:) [corrected] in a child with translocation Down syndrome
• First prenatal case of Kagami-Ogata syndrome associated with a small supernumerary marker chromosome derived from chromosome 15
• Full trisomy 14 in one of bichorionic biamniotic twins
• Genomic aberrations in pediatric gliomas and embryonal tumors
• Genotype-phenotype correlation and pregnancy outcomes of partial trisomy 14q: A systematic review
• High-level mosaic trisomy 14 at amniocentesis in a pregnancy associated with congenital heart defects and intrauterine growth restriction on fetal ultrasound
• Hyperdiploidy is less frequent in AL amyloidosis compared with monoclonal gammopathy of undetermined significance and inversely associated with translocation t(11;14)
• Imatinib Mesylate Effectiveness in Chronic Myeloid Leukemia with Additional Cytogenetic Abnormalities at Diagnosis among Black Africans
• In non-follicular lymphoproliferative disorders, IGH/BCL2-fusion is not restricted to chronic lymphocytic leukaemia
• Interphase fluorescence in situ hybridization in untreated AL amyloidosis has an independent prognostic impact by abnormality type and treatment category
• Investigation of the diagnostic value of chromosome analysis and bacterial artificial chromosome-based array comparative genomic hybridization in prenatal diagnosis
• Low-Level Trisomy 14 Mosaicism: A Carrier of an Isochromosome 14 and a Supernumerary Marker Chromosome 14
• Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability
• Molecular Delineation of Partial Trisomy 14q and Partial Trisomy 12p in a Patient with Dysmorphic Features, Heart Defect and Developmental Delay
• Monochorionic twins discordant for mosaic trisomy 14
• Mosaic trisomy 14 at amniocentesis: prenatal diagnosis and literature review
• Mosaic Trisomy 14 in a Newborn with Multiple Malformations: When Chromosomal Microarray is a Clue to Diagnosis
• Music therapy in a sleepless child with Pierre Robin sequence, partial trisomy 14 and partial monosomy 21
• Myeloid Antigen-positive T Cell Acute Lymphocytic Leukemia with t(14;18) and Trisomy 10: Report of a Case and Literature Review
• Normal prenatal ultrasound findings reflect outcome in case of trisomy 14 confined placental mosaicism developing after preimplantation genetic diagnosis
• Papillary renal cell carcinoma with cytologic and molecular genetic features overlapping with renal oncocytoma: Analysis of 10 cases
• Partial and complete trisomy 14 mosaicism: clinical follow-up, cytogenetic and molecular analysis
• Partial monosomy 7q
• Partial proximal trisomy 14: identification and molecular characterization in a girl with global developmental delay
• Partial trisomy 14q due to maternal t(4;14)(p16;q32) in a dysmorphic newborn
• Partial trisomy 9p and 14q microduplication in a patient with growth retardation: a case report and review of the literature
• Phenotypic overlapping of trisomy 12p and Pallister-Killian syndrome
• Plasma cell myeloma: role of histopathology, immunophenotyping, and genetic testing
• Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry
• Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication
• Prenatal diagnosis of partial trisomy 14q (14q31.1-->qter) and partial monosomy 5p (5p13.2-->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations
• Prenatal diagnosis of partial trisomy 3q resulting from t(3;14) in a fetus with multiple anomalies including vermian hypoplasia
• Racial differences in primary cytogenetic abnormalities in multiple myeloma: a multi-center study
• Rearrangement of chromosome 14q with associated white matter disease
• Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion
• Recurrent Cytogenetic Abnormalities in Intravascular Large B-Cell Lymphoma
• Recurrent trisomy and Robertsonian translocation of chromosome 14 in murine iPS cell lines
• Relative frequency of underlying genetic causes for the development of UPD(14)pat-like phenotype
• Road to a rare diagnosis: Description of novel unbalanced translocation causing partial trisomy 17p
• Sphincterplasty for Velopharyngeal Insufficiency in the Child Without a Cleft-Palate: Etiologies and Speech Outcomes
• Splenic marginal zone lymphoma with a de novo t(8;14)(q24;q32) and a prolymphocytoid evolution responsive to rituximab-bendamustine
• Study on genetic aberrations of ocular mucosa-associated lymphoid tissue lymphomas occurring in southern China
• Subcortical white matter abnormalities because of previously undescribed de-novo 14q12-q13.1 triplication
• t(X;14)(p11;q32) in MALT lymphoma involving GPR34 reveals a role for GPR34 in tumor cell growth
• Telomere Length Inheritance and Shortening in Trisomy 21
• Temple syndrome resulting from uniparental disomy is undiagnosed by a methylation assay due to low-level mosaicism for trisomy 14
• Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13)
• The multiple myelomas - current concepts in cytogenetic classification and therapy
• Trisomy 14 as a sole chromosome abnormality is associated with older age, a heterogenous group of myeloid neoplasms with dysplasia, and a wide spectrum of disease progression
• Trisomy 14 is a non-random karyotypic abnormality associated with myeloid malignancies
• Trisomy 14 mosaicism: clinical and cytogenetic findings in an adult
• Trisomy rescue mechanism: the case of concomitant mosaic trisomy 14 and maternal uniparental disomy 14 in a 15-year-old girl
• Two Abnormal Cell Lines of Trisomy 14 and t(X;14) with Skewed X-Inactivation
• Two cases of partial trisomy 4p and partial trisomy 14q
• Unbalanced 1q whole-arm translocation resulting in der(14)t(1;14)(q11-12;p11) in myelodysplastic syndrome
• Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis
• Uniparental disomy in Robertsonian translocations: strategies for uniparental disomy testing
• UPD(14)mat and UPD(14)mat in concomitance with mosaic small supernumerary marker chromosome 14 in two new patients with Temple syndrome
• Variation in BCL2 protein expression in follicular lymphomas without t(14;18) chromosomal translocations