BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 32467733)

  • 1. Report of trisomy 2q34-qter and monosomy 4q35.2-qter in a child with mild dysmorphic syndrome and karyotype 46,XY,der(4)t(2;4)(q34;q35.2)pat.
    Meza-Espinoza JP; Sáinz González E; León-León CJN; Arámbula-Meraz E; Contreras-Gutiérrez JA; García-Magallanes N; Madueña-Molina J; Luque-Ortega F; Cervín-Serrano S; Picos-Cárdenas VJ
    Mol Cytogenet; 2020; 13():17. PubMed ID: 32467733
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes.
    Chen CP; Lin SP; Su YN; Tsai FJ; Wu PC; Town DD; Chen LF; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2012 Mar; 51(1):93-9. PubMed ID: 22482977
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 2q34-qter duplication and 4q34.2-qter deletion in a patient with developmental delay.
    Rashidi-Nezhad A; Parvaneh N; Farzanfar F; Azimi C; Harewood L; Akrami SM; Reymond A
    Eur J Med Genet; 2012 Mar; 55(3):203-10. PubMed ID: 22370062
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cytogenomic characterization of a de novo 4q34.1 deletion in a girl with mild dysmorphic features and a coagulation disorder.
    Meza-Espinoza JP; Contreras-Gutiérrez JA; Arámbula-Meraz E; González-García JR; Domínguez-Quezada MG; García-Magallanes N; Madueña-Molina J; Benítez-Pascual J; Partida-Pérez M; Picos-Cárdenas VJ
    Mol Cytogenet; 2021 Sep; 14(1):43. PubMed ID: 34481514
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delay.
    Chen CP; Lin SP; Su YN; Chern SR; Su JW; Lee CC; Wang W
    Genet Couns; 2012; 23(4):447-55. PubMed ID: 23431743
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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.
    Paththinige CS; Sirisena ND; Kariyawasam UGIU; Ediriweera RC; Kruszka P; Muenke M; Dissanayake VHW
    BMC Med Genomics; 2018 May; 11(1):44. PubMed ID: 29739404
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: a genotype-phenotype analysis.
    Ronzoni L; Peron A; Bianchi V; Baccarin M; Guerneri S; Silipigni R; Lalatta F; Bedeschi MF
    Am J Med Genet A; 2015 Jul; 167(7):1551-9. PubMed ID: 25851921
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.
    Cervantes A; García-Delgado C; Fernández-Ramírez F; Galaz-Montoya C; Morales-Jiménez AB; Nieto-Martínez K; Gómez-Laguna L; Villa-Morales J; Quintana-Palma M; Berúmen J; Kofman S; Morán-Barroso VF
    BMC Med Genomics; 2014 Sep; 7():55. PubMed ID: 25223409
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature.
    Popescu R; Grămescu M; Caba L; Pânzaru MC; Butnariu L; Braha E; Popa S; Rusu C; Cardos G; Zeleniuc M; Martiniuc V; Gug C; Păduraru L; Stamatin M; Diaconu CC; Gorduza EV
    Genes (Basel); 2021 Dec; 12(12):. PubMed ID: 34946906
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].
    Xiao B; Ji X; Jiang WT; Zhang JM; Hu Q; Tao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):654-7. PubMed ID: 22161098
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Bilateral radial agenesis with absent thumbs, complex heart defect, short stature, and facial dysmorphism in a patient with pure distal microduplication of 5q35.2-5q35.3.
    Jamsheer A; Sowińska A; Simon D; Jamsheer-Bratkowska M; Trzeciak T; Latos-Bieleńska A
    BMC Med Genet; 2013 Jan; 14():13. PubMed ID: 23342975
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Partial monosomy 3p (3p26.2 --> pter) and partial trisomy 5q (5q34 --> qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay.
    Chen CP; Lin SP; Chen MR; Su YN; Chern SR; Liu YP; Su JW; Lee MS; Wang W
    Genet Couns; 2012; 23(3):405-13. PubMed ID: 23072190
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Genetic analysis of a case with Pierre-Robin sequence due to partial 1q trisomy and partial 4q monosomy].
    Zhang Q; Gao S; Wang L; Shi P; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Apr; 38(4):369-372. PubMed ID: 33834468
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results.
    Chen CP; Liou JD; Seow KM; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2020 Sep; 59(5):758-762. PubMed ID: 32917332
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.
    Vásquez-Velásquez AI; García-Castillo HA; González-Mercado MG; Dávalos IP; Raca G; Xu X; Dwyer E; Rivera H
    Cytogenet Genome Res; 2011; 132(4):233-8. PubMed ID: 21063078
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular cytogenetic characterization of partial monosomy 2p and trisomy 16q in a newborn: A case report.
    Yue F; Jiang Y; Pan Y; Li L; Li L; Liu R; Wang R
    Exp Ther Med; 2019 Aug; 18(2):1267-1275. PubMed ID: 31363371
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report.
    Tos T; Alp MY; Eker HK; Cebi AH; Ikbal M
    Genet Couns; 2014; 25(1):35-9. PubMed ID: 24783653
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A Very Rare Partial Trisomy Syndrome:
    Türkyılmaz A; Yaralı O
    Balkan J Med Genet; 2020 Jun; 23(1):103-108. PubMed ID: 32953418
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result.
    Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2021 Jul; 60(4):775-777. PubMed ID: 34247824
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Delineation of syndromes due to partial 6q imbalances. Trisomy 6q21 leads to qter and monosomy 6q221 leads to qter in two unrelated patients.
    Dallapiccola B; Bricarelli FD; Quartino AR; Mazzilli MC; Chisci R; Gandini E
    Acta Genet Med Gemellol (Roma); 1978; 27():57-66. PubMed ID: 751383
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.