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 *

328 related articles for article (PubMed ID: 17295347)

  • 21. Characterization of a derivative chromosome 17 by fish-technique.
    Ramesh KH; Shah HO; Sherman J; Lin JH; Verma RS
    Ann Genet; 1996; 39(3):177-80. PubMed ID: 8839891
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Prenatal diagnosis of mosaicism for triploidy and trisomy 13.
    Phelan MC; Curtis Rogers R; Michaelis RC; Moore CL; Blackburn W
    Prenat Diagn; 2001 Jun; 21(6):457-60. PubMed ID: 11438949
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal diagnosis of partial trisomy 3p (3p21-->pter) and partial monosomy 11q (11q23-->qter) associated with abnormal sonographic findings of holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system.
    Chen CP; Wang TH; Lin CC; Tsai FJ; Hsieh LJ; Wang W
    J Formos Med Assoc; 2008 Oct; 107(10):822-6. PubMed ID: 18926951
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal diagnosis of sub-microscopic partial trisomy 10q using chromosomal microarray analysis in a phenotypically abnormal fetus with normal karyotype.
    Browne PC; Adam S; Badr M; Brooks CR; Edwards J; Walker P; Mohamed S; Gregg AR
    J Neonatal Perinatal Med; 2016 May; 9(2):217-22. PubMed ID: 27197934
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly.
    Chen CP; Wang LK; Chern SR; Wu PS; Ko K; Chen YN; Chen SW; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2016 Aug; 55(4):591-5. PubMed ID: 27590389
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis of a partial 6q trisomy: a case report.
    Valerio D; Di Domenico A; Felicetti M; La Boccetta A; Ferrara C; Antonio N; Borrelli AL
    Prenat Diagn; 2006 Oct; 26(10):917-9. PubMed ID: 16845680
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints.
    Chen CP; Chang YL; Chern SR; Wu PS; Su JW; Chen WL; Chen LF; Wang W
    Gene; 2013 Mar; 516(1):132-7. PubMed ID: 23266805
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal diagnosis of 47,XX,der(15)t(15;16)(q13;p13.2).
    Santolaya-Forgas J; De Leon J; Powell WC; Tonk V
    Prenat Diagn; 2004 Mar; 24(3):209-12. PubMed ID: 15057955
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31 →qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization.
    Chen CP; Su YN; Young RS; Tsai FJ; Wu PC; Chern SR; Town DD; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):506-12. PubMed ID: 21199755
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: description in a boy with partial trisomy 10q and monosomy 4q and review of the literature.
    Bartholdi D; Toelle SP; Steiner B; Boltshauser E; Schinzel A; Riegel M
    Eur J Med Genet; 2008; 51(2):113-23. PubMed ID: 18262484
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
    Kímya Y; Yakut T; Egelí U; Ozerkan K
    Prenat Diagn; 2002 Nov; 22(11):957-61. PubMed ID: 12424755
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Prenatal diagnosis of monosomy 4p14-->pter and trisomy 11q25-->qter: clinical presentations and outcomes.
    Peng HH; Wang TH; Chao AS; Chang YL; Chang SD; Soong YK
    Prenat Diagn; 2005 Dec; 25(12):1133-7. PubMed ID: 16231301
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Partial trisomy 10q: further delineation of the clinical manifestations involving the segment 10q23-->10q24.
    Halpern GJ; Shohat M; Merlob P
    Ann Genet; 1996; 39(3):181-3. PubMed ID: 8839892
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
    Chen CP; Lin SP; Chern SR; Shih SL; Lee CC; Wang W; Liao YW
    Prenat Diagn; 2003 Jun; 23(6):504-8. PubMed ID: 12813767
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prenatal diagnosis of trisomy 4p: a new locus for holoprosencephaly?
    Karmous-Benailly H; Tabet AC; Thaly A; Dupuy O; Huten Y; Luton D; Baumann C; Delezoide AL
    Prenat Diagn; 2005 Mar; 25(3):193-7. PubMed ID: 15791668
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatal diagnosis and prenatal imaging features of fetal monosomy 1p36.
    Lissauer D; Larkins SA; Sharif S; MacPherson L; Rhodes C; Kilby MD
    Prenat Diagn; 2007 Sep; 27(9):874-8. PubMed ID: 17582615
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
    Chen CP; Chern SR; Lee CC; Chang TY; Wang W; Tzen CY
    Prenat Diagn; 2004 Jan; 24(1):38-44. PubMed ID: 14755408
    [TBL] [Abstract][Full Text] [Related]  

  • 38. DiGeorge syndrome and partial monosomy 10p: case report and review.
    Schuffenhauer S; Seidel H; Oechsler H; Belohradsky B; Bernsau U; Murken J; Meitinger T
    Ann Genet; 1995; 38(3):162-7. PubMed ID: 8540688
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).
    Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Chern SR; Lee CC; Chen YJ; Wang W
    Prenat Diagn; 2005 Dec; 25(12):1170-2. PubMed ID: 16315335
    [No Abstract]   [Full Text] [Related]  

  • 40. Partial trisomy 3q in a child with sacrococcygeal teratoma and Cornelia de Lange syndrome phenotype.
    Dundar M; Uzak A; Erdogan M; Saatci C; Akdeniz S; Luleci G; Keser I; Karauzum S
    Genet Couns; 2011; 22(2):199-205. PubMed ID: 21848013
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.