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

140 related items for PubMed ID: 12476455

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype.
    Tihy F, Lemyre E, Lemieux N, Dallaire L.
    Am J Med Genet; 1999 Dec 03; 87(4):302-5. PubMed ID: 10588834
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Xq chromosome duplication in males: clinical, cytogenetic and array CGH characterization of a new case and review.
    Cheng SF, Rauen KA, Pinkel D, Albertson DG, Cotter PD.
    Am J Med Genet A; 2005 Jun 15; 135(3):308-13. PubMed ID: 15887264
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Functional disomy for Xq22-q23 in a girl with complex rearrangements of chromosomes 3 and X.
    Ida T, Miharu N, Hayashitani M, Shimokawa O, Harada N, Samura O, Kubota T, Niikawa N, Matsumoto N.
    Am J Med Genet A; 2003 Aug 01; 120A(4):557-61. PubMed ID: 12884439
    [Abstract] [Full Text] [Related]

  • 13. Duplication of the short arm of the X chromosome in mother and daughter.
    Tuck-Muller CM, Martinez JE, Batista DA, Kearns WG, Wertelecki W.
    Hum Genet; 1993 May 01; 91(4):395-400. PubMed ID: 8500796
    [Abstract] [Full Text] [Related]

  • 14. De novo duplication xq22-q23 in a girl with short stature and gonadal dysgenesis.
    Correa-Cerro L, Garcia-Cruz D, Ruiz MX, Sanchez-Corona J.
    Ann Genet; 1999 May 01; 42(1):41-4. PubMed ID: 10214506
    [Abstract] [Full Text] [Related]

  • 15. Identification of a de novo inv dup(X)(pter--> q22) by multicolor banding in a girl with Turner syndrome.
    Burégio-Frota P, Valença L, Leal GF, Duarte AR, Bispo-Brito AV, Soares-Ventura EM, Marques-Salles TJ, Nogueira MT, Muniz MT, Silva ML, Hunstig F, Liehr T, Santos N.
    Genet Mol Res; 2010 Apr 27; 9(2):780-4. PubMed ID: 20449811
    [Abstract] [Full Text] [Related]

  • 16. Cryptic x; autosome translocation in a boy--delineation of the phenotype.
    Jezela-Stanek A, Ciara E, Juszczak M, Pelc M, Materna-Kiryluk A, Krajewska-Walasek M.
    Pediatr Neurol; 2011 Mar 27; 44(3):221-4. PubMed ID: 21310340
    [Abstract] [Full Text] [Related]

  • 17. Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation.
    Stankiewicz P, Kuechler A, Eller CD, Sahoo T, Baldermann C, Lieser U, Hesse M, Gläser C, Hagemann M, Yatsenko SA, Liehr T, Horsthemke B, Claussen U, Marahrens Y, Lupski JR, Hansmann I.
    Am J Med Genet A; 2006 Mar 01; 140(5):442-52. PubMed ID: 16470732
    [Abstract] [Full Text] [Related]

  • 18. Birth of a healthy child by a woman with inherited Xq duplications who had experienced stillbirths.
    Dong Y, Chen SC, Yu XW, Fadlalla E, Jin F, Liu RZ.
    Genet Mol Res; 2014 Jun 17; 13(2):4573-8. PubMed ID: 25036506
    [Abstract] [Full Text] [Related]

  • 19. Sex reversal from functional disomy of Xp: prenatal and post-mortem findings.
    Piccione M, Maresi E, Zollino M, Sanfilippo C, Seminara L, Neri G, Corsello G.
    Am J Med Genet A; 2008 Oct 15; 146A(20):2681-7. PubMed ID: 18798322
    [Abstract] [Full Text] [Related]

  • 20. Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions.
    El-Hattab AW, Fang P, Jin W, Hughes JR, Gibson JB, Patel GS, Grange DK, Manwaring LP, Patel A, Stankiewicz P, Cheung SW.
    J Med Genet; 2011 Dec 15; 48(12):840-50. PubMed ID: 21984752
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.