BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 35595446)

  • 1. Prenatal diagnosis and molecular cytogenetic characterization of partial dup (18p)/del (18q) due to a maternal pericentric inversion 18 in a foetus with multiple anomalies.
    Atli EI; Atli E; Inan C; Varol GF; Mail C; Erbilen EA; Yalcintepe S; Demir S; Gurkan H
    Taiwan J Obstet Gynecol; 2022 May; 61(3):504-509. PubMed ID: 35595446
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del(18p) recombinant chromosome.
    Vermeulen SJ; Speleman F; Vanransbeeck L; Verspeet J; Menten B; Verschraegen-Spae MR; Wilde PD; Messiaen L; Michaelis RC; Leroy JG
    Eur J Hum Genet; 2005 Jan; 13(1):52-8. PubMed ID: 15470365
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction.
    Chen CP; Ko TM; Huang WC; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Pan CW; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Jun; 55(3):415-8. PubMed ID: 27343326
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18)dup(18q)inv(18)(p11.31q11.2)mat.
    Leonard NJ; Tomkins DJ; Demianczuk N
    Prenat Diagn; 2000 Dec; 20(12):947-9. PubMed ID: 11113905
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
    Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13).
    Yakut S; Cetin Z; Sanhal C; Karaman B; Mendilcioglu I; Karauzum SB
    Genet Couns; 2015; 26(2):243-7. PubMed ID: 26349196
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.
    Prabhakara K; Wyandt HE; Huang XL; Prasad KS; Ramadevi AR
    Ann Genet; 2004; 47(3):297-303. PubMed ID: 15337476
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular cytogenetic characterization of del(X)(p22.33)mat and de novo dup(4)(q34.3q35.2) in a male fetus with multiple anomalies of facial dysmorphism, ventriculomegaly, congenital heart defects, short long bones and clinodactyly.
    Chen CP; Huang JP; Chen YY; Chen SW; Chern SR; Wu PS; Wu FT; Pan YT; Chen WL; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2023 May; 62(3):453-456. PubMed ID: 37188453
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly.
    Chen CP; Kuo YK; Su YN; Chern SR; Tsai FJ; Wu PC; Chen YT; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):182-7. PubMed ID: 21791305
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3).
    Asano T; Ikeuchi T; Shinohara T; Enokido H; Hashimoto K
    Jinrui Idengaku Zasshi; 1991 Sep; 36(3):257-65. PubMed ID: 1753439
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Low-level complex mosaic with multiple cell lines affecting the 18q21.31q21.32 region in a patient with de novo 18q terminal deletion.
    Bonaglia MC; Fichera M; Marelli S; Romaniello R; Zuffardi O
    Eur J Med Genet; 2022 Nov; 65(11):104596. PubMed ID: 36064004
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal diagnosis of 18p deletion and isochromosome 18q mosaicism in a fetus with a cystic hygroma.
    Vičić A; Hafner T; Wagner J; Stipoljev F
    Coll Antropol; 2014 Sep; 38(3):1059-62. PubMed ID: 25420396
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
    Chen CP; Su YN; Chern SR; Hsu CY; Tsai FJ; Wu PC; Lee CC; Chen YT; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2011 Mar; 50(1):67-73. PubMed ID: 21482378
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.