These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 29090019)

  • 1. Molecular characterization and evaluation of complex rearrangements in a case of ring chromosome 15.
    Tewari S; Lubna N; Shah R; Al-Rikabi ABH; Shah K; Sheth J; Sheth F
    Mol Cytogenet; 2017; 10():38. PubMed ID: 29090019
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation.
    Chen CP; Lin SP; Chern SR; Wu PS; Su JW; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2014 Mar; 53(1):74-8. PubMed ID: 24767651
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Haploinsufficiency and triploinsensitivity of the same 6p25.1p24.3 region in a family.
    Qi Z; Jeng LJ; Slavotinek A; Yu J
    BMC Med Genomics; 2015 Jul; 8():38. PubMed ID: 26174853
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis of 1p34.3 interstitial microdeletion by aCGH in a fetus with jaw bone abnormalities.
    Dagklis T; Papageorgiou E; Siomou E; Paspaliaris V; Zerva C; Chatzis P; Thomaidis L; Manolakos E; Papoulidis I
    Mol Cytogenet; 2016; 9():77. PubMed ID: 27713767
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 46,XY,r(8)/45,XY,-8 Mosaicism as a Possible Mechanism of the Imprinted Birk-Barel Syndrome: A Case Study.
    Kashevarova AA; Nikitina TV; Mikhailik LI; Belyaeva EO; Vasilyev SA; Lopatkina ME; Fedotov DA; Fonova EA; Zarubin AA; Sivtsev AA; Skryabin NA; Nazarenko LP; Lebedev IN
    Genes (Basel); 2020 Dec; 11(12):. PubMed ID: 33316910
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ring chromosome 15: characterization by array CGH.
    Glass IA; Rauen KA; Chen E; Parkes J; Alberston DG; Pinkel D; Cotter PD
    Hum Genet; 2006 Jan; 118(5):611-7. PubMed ID: 16267671
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.
    Chen CP; Tsai CH; Chern SR; Wu PS; Su JW; Lee CC; Chen YT; Chen WL; Chen LF; Wang W
    Gene; 2013 Oct; 529(1):163-8. PubMed ID: 23933417
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.
    Chen CP; Ko TM; Su YN; Wang LK; Chern SR; Wu PS; Chen YN; Chen SW; Ko K; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):733-737. PubMed ID: 27751426
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Molecular cytogenetic study of a case with ring chromosome 15].
    Zhang J; Yang Y; Zhang J; Wang S; Yao F; Zhang Y; Jiang S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar; 38(3):238-241. PubMed ID: 33751532
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome.
    Girirajan S; Williams S; Garbern J; Nowak N; Hatchwell E; Elsea S
    Clin Genet; 2007 Jul; 72(1):47-58. PubMed ID: 17594399
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of 21q22.3.
    Chen CP; Lin YH; Chou SY; Su YN; Chern SR; Chen YT; Town DD; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2012 Mar; 51(1):71-6. PubMed ID: 22482972
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A child with intellectual disability and dysmorphism due to complex ring chromosome 6: identification of molecular mechanism with review of literature.
    Sheth F; Liehr T; Shah V; Shah H; Tewari S; Solanki D; Trivedi S; Sheth J
    Ital J Pediatr; 2018 Oct; 44(1):114. PubMed ID: 30305128
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency.
    Chen CP; Lin CJ; Chen YN; Chern SR; Chen SW; Lai ST; Wu PS; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2017 Jun; 56(3):398-401. PubMed ID: 28600059
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An 800  kb deletion at 17q23.2 including the MED13 (THRAP1) gene, revealed by aCGH in a patient with a SMC 17p.
    Boutry-Kryza N; Labalme A; Till M; Schluth-Bolard C; Langue J; Turleau C; Edery P; Sanlaville D
    Am J Med Genet A; 2012 Feb; 158A(2):400-5. PubMed ID: 22162340
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.
    Chen CP; Lin SP; Lin YH; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):852-855. PubMed ID: 28040132
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.
    Chen CP; Chen M; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chang SP; Yang CW; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Aug; 56(4):527-533. PubMed ID: 28805612
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
    Chen CP; Chen M; Ko TM; Ma GC; Tsai FJ; Tsai MS; Wu PC; Lee CC; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):500-5. PubMed ID: 21199754
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3).
    Chen CP; Lin YH; Au HK; Su YN; Hsu CY; Liu YP; Wu PC; Chern SR; Chen YT; Chen LF; Hsieh AH; Wang W
    Taiwan J Obstet Gynecol; 2011 Sep; 50(3):359-65. PubMed ID: 22030053
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Combined spectral karyotyping and microarray-based comparative genomic hybridization for the diagnosis of a case with ring chromosome 15].
    Pan M; Choy KW; Liao C; Lau TK
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct; 29(5):562-5. PubMed ID: 23042394
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.