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 *

182 related articles for article (PubMed ID: 21932318)

  • 41. Three patients with hallucal polydactyly and WAGR syndrome, including discordant expression of Wilms tumor in MZ twins.
    Brémond-Gignac D; Gérard-Blanluet M; Copin H; Bitoun P; Baumann C; Crolla JA; Benzacken B; Verloes A
    Am J Med Genet A; 2005 May; 134(4):422-5. PubMed ID: 15779023
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Familial presentation of microdeletion and inverted microduplication with array-CGH].
    Beseler-Soto B; Jiménez-Candel MI; Pedrón-Marzal G; Pérez-García B; Carpena-Lucas PJ
    Rev Neurol; 2014 Dec; 59(12):551-4. PubMed ID: 25501453
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Parental imbalances involving chromosomes 15q and 22q may predispose to the formation of de novo pathogenic microdeletions and microduplications in the offspring.
    Capra V; Mascelli S; Garrè ML; Nozza P; Vaccari C; Bricco L; Sloan-Béna F; Gimelli S; Cuoco C; Gimelli G; Tassano E
    PLoS One; 2013; 8(3):e57910. PubMed ID: 23483941
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions.
    Bi W; Cheung SW; Breman AM; Bacino CA
    Am J Med Genet A; 2016 Oct; 170(10):2540-50. PubMed ID: 27287194
    [TBL] [Abstract][Full Text] [Related]  

  • 45. WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletion.
    Huynh MT; Boudry-Labis E; Duban B; Andrieux J; Tran CT; Tampere H; Ceraso D; Manouvrier S; Tachdjian G; Roche-Lestienne C; Vincent-Delorme C
    Am J Med Genet A; 2017 Jun; 173(6):1690-1693. PubMed ID: 28398607
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
    Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
    J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
    [TBL] [Abstract][Full Text] [Related]  

  • 47. A de novo 8q22.2-24.3 duplication in a patient with mild phenotype.
    Concolino D; Iembo MA; Moricca MT; Rapsomaniki M; Marotta R; Galesi O; Fichera M; Romano C; Strisciuglio P
    Eur J Med Genet; 2012 Jan; 55(1):67-70. PubMed ID: 21971480
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation.
    Chen CP; Lin SP; Chern SR; Wu PS; Su JW; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2014 Mar; 53(1):74-8. PubMed ID: 24767651
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Characterization of a de novo duplication of 11p14----p13, using fluorescent in situ hybridization and southern hybridization.
    Speleman F; Mannens M; Redeker B; Vercruyssen M; Van Oostveldt P; Leroy J; Slater R
    Cytogenet Cell Genet; 1991; 56(3-4):129-31. PubMed ID: 2055105
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Array CGH detection of a novel cryptic deletion at 3q13 in a complex chromosome rearrangement.
    López-Expósito I; Ballesta-Martinez MJ; Bafalliu JA; Vera-Carbonell A; Domingo-Jiménez R; López-González V; Fernández A; Guillén-Navarro E
    Genomics; 2014 Apr; 103(4):288-91. PubMed ID: 24607569
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
    Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
    Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Clinical and genomic characterization of siblings with a distal duplication of chromosome 9q (9q34.1-qter).
    Mizuno S; Fukushi D; Kimura R; Yamada K; Yamada Y; Kumagai T; Wakamatsu N
    Am J Med Genet A; 2011 Sep; 155A(9):2274-80. PubMed ID: 21834029
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature.
    Recalcati MP; Bellini M; Norsa L; Ballarati L; Caselli R; Russo S; Larizza L; Giardino D
    Gene; 2012 Jul; 502(1):40-5. PubMed ID: 22537675
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Inheritance of a terminal 7.1 Mb 18p deletion flanked by a 2.3 Mb duplication from a physically normal mother.
    Misceo D; Orstavik KH; Lybaek H; Sandvig I; Ormerod E; Houge G; Frengen E
    Am J Med Genet A; 2009 Dec; 149A(12):2877-81. PubMed ID: 19938092
    [No Abstract]   [Full Text] [Related]  

  • 55. A rare case of trisomy 11q23.3-11q25 and trisomy 22q11.1-22q11.21.
    Zou PS; Li HF; Chen LS; Ma M; Chen XH; Xue D; Cao DH
    Genet Mol Res; 2016 May; 15(2):. PubMed ID: 27173335
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
    Chen CP; Kuo YT; Lin SP; Su YN; Chen YJ; Hsueh RY; Lin YH; Wu PC; Lee CC; Chen YT; Wang W
    Taiwan J Obstet Gynecol; 2010 Sep; 49(3):327-32. PubMed ID: 21056319
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Pure duplication of 19p13.3.
    Ishikawa A; Enomoto K; Tominaga M; Saito T; Nagai J; Furuya N; Ueno K; Ueda H; Masuno M; Kurosawa K
    Am J Med Genet A; 2013 Sep; 161A(9):2300-4. PubMed ID: 23897601
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Array comparative genomic hybridization analysis of a familial duplication of chromosome 13q: a recognizable syndrome.
    Mathijssen IB; Hoovers JM; Mul AN; Man HY; Ket JL; Hennekam RC
    Am J Med Genet A; 2005 Jul; 136(1):76-80. PubMed ID: 15889415
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Chromosomal location of submicroscopic duplications in patients with neurodevelopmental disorders to identify cases with high risk of familial recurrence].
    López-Carrasco A; Monfort S; Roselló M; Oltra S; Mayo S; Martínez F; Orellana C
    Med Clin (Barc); 2014 Jun; 142(12):531-7. PubMed ID: 23790573
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Craniofacial and Neurological Phenotype in a Patient with De Novo 18q Microdeletion and 18p Microduplication.
    Yapijakis C; Angelopoulou A; Manolakos E; Voumvourakis C
    Adv Exp Med Biol; 2020; 1195():163-166. PubMed ID: 32468472
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.