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 *

164 related articles for article (PubMed ID: 32803851)

  • 1. Pre- and postnatal findings in a patient with a recombinant chromosome rec(8)(qter→q21.11::p23.3→qter) due to a paternal pericentric inversion inv(8)(p23.3q21.11) and review of the literature.
    Habhab W; Mau-Holzmann U; Singer S; Rieß A; Kagan KO; Gerbig I; Schäferhoff K; Dufke A; Kehrer M
    Am J Med Genet A; 2020 Nov; 182(11):2680-2684. PubMed ID: 32803851
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pre- and postnatal findings in a patient with a novel rec(8)dup(8q)inv(8)(p23.2q22.3) associated with San Luis Valley syndrome.
    Vera-Carbonell A; López-González V; Bafalliu JA; Piñero-Fernández J; Susmozas J; Sorli M; López-Pérez R; Fernández A; Guillén-Navarro E; López-Expósito I
    Am J Med Genet A; 2013 Sep; 161A(9):2369-75. PubMed ID: 23894102
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cloning, sequencing, and analysis of inv8 chromosome breakpoints associated with recombinant 8 syndrome.
    Graw SL; Sample T; Bleskan J; Sujansky E; Patterson D
    Am J Hum Genet; 2000 Mar; 66(3):1138-44. PubMed ID: 10712224
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular cytogenetic characterization of a derivative chromosome 8 with an inverted duplication of 8p21.3-->p23.3 and a rearranged duplication of 8q24.13-->qter.
    Fan YS; Siu VM
    Am J Med Genet; 2001 Aug; 102(3):266-71. PubMed ID: 11484205
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular cytogenetic analysis and clinical findings in a newborn with prenatally diagnosed rec(7)dup(7q)inv(7)(p22q31.3)pat.
    Goodman BK; Stone K; Coddett JM; Cargile CB; Gurewitsch ED; Blakemore KJ; Stetten G
    Prenat Diagn; 1999 Dec; 19(12):1150-6. PubMed ID: 10590434
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
    Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
    Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Structural abnormalities of chromosome 8 and fetoplacental discrepancy: A second case report and review of fetal phenotype of 8p inverted duplication deletion syndrome.
    Huynh MT; Riteau AS; Moradkhani K; Pichon O; Richard S; Joubert M; Bézieau S
    Eur J Med Genet; 2021 Jan; 64(1):104118. PubMed ID: 33248287
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Clinical phenotype and genetic analysis of a fetus with recombinant chromosome 8 syndrome].
    Hao W; Zhang Y; Wang Y; Xie L; Yu X; Lyu J; Che Y; Xu J; Jia Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):1036-1040. PubMed ID: 37532508
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.
    Guo WJ; Callif-Daley F; Zapata MC; Miller ME
    Am J Med Genet; 1995 Sep; 58(3):230-6. PubMed ID: 8533823
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Duplication of 20qter and deletion of 20pter due to paternal pericentric inversion: patient report and review of 20qter duplications.
    Starr LJ; Truemper EJ; Pickering DL; Sanger WG; Olney AH
    Am J Med Genet A; 2014 Aug; 164A(8):2020-4. PubMed ID: 24954807
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Lee MS; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):705-711. PubMed ID: 27751420
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).
    Allderdice PW; Browne N; Murphy DP
    Am J Hum Genet; 1975 Nov; 27(6):699-718. PubMed ID: 1200027
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Inverted duplication of the short arm of chromosome 8].
    Rodríguez Martínez L; Jiménez Muñoz-Delgado N; Nieto C; Martínez Carrascal A; López Grondona F; Martínez Frías ML
    An Esp Pediatr; 2001 Nov; 55(5):458-62. PubMed ID: 11696311
    [TBL] [Abstract][Full Text] [Related]  

  • 14. dup(8p)/del(8q) recombinant chromosome in a girl with hepatic focal nodular hyperplasia.
    Tokutomi T; Hayashi S; Imai K; Chida A; Ishiwata T; Asano Y; Inazawa J; Nonoyama S
    Am J Med Genet A; 2007 Jun; 143A(12):1334-7. PubMed ID: 17506094
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Partial deletion of 18p and partial duplication of 18q caused by a paternal pericentric inversion.
    Israëls T; Hoovers J; Turpijn HM; Wijburg FA; Hennekam RC
    Clin Genet; 1996 Dec; 50(6):520-4. PubMed ID: 9147887
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of a recombinant chromosome 7 resulting in trisomy 7q11.22 --> qter.
    Tchirikov M; Merinsky A; Strohner M; Bonin M; Beyer V; Haaf T; Bartsch O
    Am J Med Genet A; 2010 Mar; 152A(3):721-5. PubMed ID: 20186810
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Duplication of the segment q12.2 leads to qter of chromosome 22 due to paternal inversion 22(p13q12.2).
    Fujimoto A; Wilson MG; Towner JW
    Hum Genet; 1983; 63(1):82-4. PubMed ID: 6832783
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new case of partial 14q31.3-qter trisomy due to maternal pericentric inversion.
    Sgardioli IC; Simioni M; Viguetti-Campos NL; Prota JR; Gil-da-Silva-Lopes VL
    Gene; 2013 Jul; 523(2):192-4. PubMed ID: 23566844
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies.
    Lee MJ; Park SH; Shim SH; Moon MJ; Cha DH
    Taiwan J Obstet Gynecol; 2019 May; 58(3):318-323. PubMed ID: 31122516
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.