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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

211 related items for PubMed ID: 30945692

  • 1. A small supernumerary marker chromosome resulting in mosaic partial tetrasomy 4q26-q31.21 in a foetus with multiple congenital malformations.
    Zhang ZT, Qi WX, Liu CX, Yin SW, Zhao Y, Li-Ling J, Lv Y.
    J Genet; 2019 Mar; 98():. PubMed ID: 30945692
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome (sSMC) inherited from her mosaic sSMC(15) mother and a literature review.
    Sun ML, Zhang HG, Liu XY, Yue FG, Jiang YT, Li SB, Liu RZ.
    Taiwan J Obstet Gynecol; 2020 Nov; 59(6):963-967. PubMed ID: 33218423
    [Abstract] [Full Text] [Related]

  • 4. Diagnosis and clinical delineation of mosaic tetrasomy 5p.
    Blakey-Cheung S, Parker P, Schlaff W, Monseur B, Keppler-Noreuil K, Al-Kouatly HB.
    Eur J Med Genet; 2020 Jan; 63(1):103634. PubMed ID: 30797979
    [Abstract] [Full Text] [Related]

  • 5. Mosaic Tetrasomy of 9p24.3q21.11 postnatally identified in an infant born with multiple congenital malformations: a case report.
    Pinto IP, Minasi LB, Steckelberg R, da Silva CC, da Cruz AD.
    BMC Pediatr; 2018 Sep 07; 18(1):298. PubMed ID: 30193577
    [Abstract] [Full Text] [Related]

  • 6. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome.
    Chen CP, Ko TM, Chen YY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2017 Dec 07; 56(6):836-839. PubMed ID: 29241930
    [Abstract] [Full Text] [Related]

  • 7. Tetrasomy 13q31.1qter due to an inverted duplicated neocentric marker chromosome in a fetus with multiple malformations.
    Haddad V, Aboura A, Tosca L, Guediche N, Mas AE, L'Herminé AC, Druart L, Picone O, Brisset S, Tachdjian G.
    Am J Med Genet A; 2012 Apr 07; 158A(4):894-900. PubMed ID: 22419357
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.
    Chen CP, Ko TM, Chern SR, Wu PS, Chen SW, Lai ST, Yang CW, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2017 Aug 07; 56(4):545-549. PubMed ID: 28805616
    [Abstract] [Full Text] [Related]

  • 9. Mosaic complete tetrasomy 21 in a fetus with complete atrioventricular septal defect and minor morphological variations.
    Gatinois V, Bigi N, Mousty E, Chiesa J, Musizzano Y, Schneider A, Lefort G, Pinson L, Gaillard JB, Ragon C, Perez MJ, Tournaire M, Blanchet P, Corsini C, Haquet E, Callier P, Geneviève D, Pellestor F, Puechberty J.
    Mol Genet Genomic Med; 2019 Nov 07; 7(11):e00895. PubMed ID: 31493343
    [Abstract] [Full Text] [Related]

  • 10. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review.
    Chen CP, Chen M, Wu CH, Lin CJ, Chern SR, Wu PS, Chen YN, Chen SW, Chang SP, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2017 Aug 07; 56(4):554-557. PubMed ID: 28805618
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.
    Chen CP, Chern SR, Chang TY, Lee CC, Chen LF, Tzen CY, Wang W, Lin CJ, Yang BP, Yang LS.
    Prenat Diagn; 2003 Jan 07; 23(1):40-3. PubMed ID: 12533811
    [Abstract] [Full Text] [Related]

  • 12. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
    Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ.
    Prenat Diagn; 2006 Oct 07; 26(10):898-902. PubMed ID: 16915592
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality.
    Chen CP, Chern SR, Chen YN, Chen SW, Wu PS, Yang CW, Lee CC, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2017 Apr 07; 56(2):217-223. PubMed ID: 28420511
    [Abstract] [Full Text] [Related]

  • 14. Prenatal diagnosis of mosaic tetrasomy 5p.
    Park JP, Barefoot KH, Ornvold K, Berg SZ, Dossu JR, Mohandas TK.
    Prenat Diagn; 2001 May 07; 21(5):351-3. PubMed ID: 11360274
    [Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis of a mosaic supernumerary marker iso (8p) (tetrasomy 8p): discordance between chorionic villi culture and amniotic fluid karyotypes.
    Nucaro AL, Rossino R, Pruna D, Rassu S, Cianchetti C, Cao A, Moi P.
    Prenat Diagn; 2006 May 07; 26(5):418-9. PubMed ID: 16532523
    [Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11.
    Chen CP, Chen M, Wang PT, Chern SR, Chen SW, Lai ST, Wu PS, Chang SP, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2017 Jun 07; 56(3):394-397. PubMed ID: 28600058
    [Abstract] [Full Text] [Related]

  • 17. Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay.
    Chen CP, Chiang S, Wang KL, Cho FN, Chen M, Chern SR, Wu PS, Chen YN, Chen SW, Chang SP, Chen WL, Wang W.
    Taiwan J Obstet Gynecol; 2016 Jun 07; 55(3):419-22. PubMed ID: 27343327
    [Abstract] [Full Text] [Related]

  • 18. Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13.
    Tonnies H, Gerlach A, Heineking B, Starke H, Neitzel H, Neumann LM.
    Cytogenet Genome Res; 2006 Jun 07; 114(3-4):325-9. PubMed ID: 16954674
    [Abstract] [Full Text] [Related]

  • 19. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.
    Levy B, Papenhausen P, Tepperberg J, Dunn T, Fallet S, Magid M, Kardon N, Hirschhorn K, Warburton P.
    Cytogenet Cell Genet; 2000 Jun 07; 91(1-4):165-70. PubMed ID: 11173851
    [Abstract] [Full Text] [Related]

  • 20. Tetrasomy 15q25.2→qter identified with SNP microarray in a patient with multiple anomalies including complex cardiovascular malformation.
    George-Abraham JK, Zimmerman SL, Hinton RB, Marino BS, Witte DP, Hopkin RJ.
    Am J Med Genet A; 2012 Aug 07; 158A(8):1971-6. PubMed ID: 22711292
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.