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 *

141 related articles for article (PubMed ID: 31478360)

  • 1. Inverted duplication, triplication and quintuplication through sequential breakage-fusion-bridge events induced by a terminal deletion at 5p in a case of spontaneous abortion.
    Chai H; Grommisch B; DiAdamo A; Wen J; Hui P; Li P
    Mol Genet Genomic Med; 2019 Oct; 7(10):e00965. PubMed ID: 31478360
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spectrum of Cytogenomic Abnormalities Revealed by Array Comparative Genomic Hybridization on Products of Conception Culture Failure and Normal Karyotype Samples.
    Zhou Q; Wu SY; Amato K; DiAdamo A; Li P
    J Genet Genomics; 2016 Mar; 43(3):121-31. PubMed ID: 27020032
    [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 mosaicism for a distal 5p deletion in a single colony at amniocentesis in a pregnancy with a favorable outcome and a review of mosaic distal 5p deletion.
    Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2020 Mar; 59(2):334-337. PubMed ID: 32127161
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detection of a rare de novo 18p terminal deletion with inverted duplication in a Chinese pregnant woman.
    Zhu J; Qi H; Cao S; Cai L; Wen X; Tang G; Wan Q; Chen C; Wang J; Zeng W; Luo Y
    Mol Genet Genomic Med; 2019 Sep; 7(9):e868. PubMed ID: 31317671
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication.
    Chen CP; Huang JP; Chern SR; Wu PS; Chen SW; Wu FT; Chen WL; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2020 Jan; 59(1):140-145. PubMed ID: 32039783
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Telomere capture as a frequent mechanism for stabilization of the terminal chromosomal deletion associated with inverted duplication.
    Yu S; Graf WD
    Cytogenet Genome Res; 2010; 129(4):265-74. PubMed ID: 20606397
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Post-zygotic breakage of a dicentric chromosome results in mosaicism for a telocentric 9p marker chromosome in a boy with developmental delay.
    Pedurupillay CR; Misceo D; Gamage TH; Dissanayake VH; Frengen E
    Gene; 2014 Jan; 533(1):403-10. PubMed ID: 24095780
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages.
    Schaeffer AJ; Chung J; Heretis K; Wong A; Ledbetter DH; Lese Martin C
    Am J Hum Genet; 2004 Jun; 74(6):1168-74. PubMed ID: 15127362
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization.
    Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2019 Sep; 58(5):698-703. PubMed ID: 31542096
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement.
    Preiksaitiene E; Benušienė E; Ciuladaite Z; Šliužas V; Mikštienė V; Kučinskas V
    Taiwan J Obstet Gynecol; 2016 Jun; 55(3):410-4. PubMed ID: 27343325
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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.
    Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
    Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11.
    Hu J; Sathanoori M; Kochmar S; Madan-Khetarpal S; McGuire M; Surti U
    Am J Med Genet A; 2013 Jan; 161A(1):179-84. PubMed ID: 23225375
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Array CGH characterization of an unbalanced X-autosome translocation associated with Xq27.2-qter deletion, 11q24.3-qter duplication and Xq22.3-q27.1 duplication in a girl with primary amenorrhea and mental retardation.
    Chen CP; Lin SP; Chern SR; Kuo YL; Wu PS; Chen YT; Lee MS; Wang W
    Gene; 2014 Feb; 535(1):88-92. PubMed ID: 24279999
    [TBL] [Abstract][Full Text] [Related]  

  • 17. U-type exchange is the most frequent mechanism for inverted duplication with terminal deletion rearrangements.
    Rowe LR; Lee JY; Rector L; Kaminsky EB; Brothman AR; Martin CL; South ST
    J Med Genet; 2009 Oct; 46(10):694-702. PubMed ID: 19293169
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Unique genomic structure and distinct mitotic behavior of ring chromosome 21 in two unrelated cases.
    Zhang HZ; Xu F; Seashore M; Li P
    Cytogenet Genome Res; 2012; 136(3):180-7. PubMed ID: 22398511
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Integrated FISH, Karyotyping and aCGH Analyses for Effective Prenatal Diagnosis of Common Aneuploidies and Other Cytogenomic Abnormalities.
    Chai H; DiAdamo A; Grommisch B; Boyle J; Amato K; Wang D; Wen J; Li P
    Med Sci (Basel); 2019 Jan; 7(2):. PubMed ID: 30678103
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Application of array-based comparative genomic hybridization technique in genetic analysis of patients with spontaneous abortion].
    Chu Y; Wu D; Hou QF; Huo XD; Gao Y; Wang T; Wang HD; Yang YL; Liao SX
    Zhonghua Fu Chan Ke Za Zhi; 2016 Aug; 51(8):592-6. PubMed ID: 27561938
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.