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    Results: 1 to 20 of 166

    1.

    11p Microdeletion including WT1 but not PAX6, presenting with cataract, mental retardation, genital abnormalities and seizures: a case report.

    Almind GJ, Brøndum-Nielsen K, Bangsgaard R, Baekgaard P, Grønskov K.

    Mol Cytogenet. 2009 Feb 17;2:6.PMID: 19222835 [PubMed - in process]Free PMC ArticleFree textRelated citations

    2.

    Combination of WAGR and Potocki-Shaffer contiguous deletion syndromes in a patient with an 11p11.2-p14 deletion.

    Brémond-Gignac D, Crolla JA, Copin H, Guichet A, Bonneau D, Taine L, Lacombe D, Baumann C, Benzacken B, Verloes A.

    Eur J Hum Genet. 2005 Apr;13(4):409-13.PMID: 15702131 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

    3.

    Aniridia.

    Hingorani M, Moore A

    In: Pagon RA, Bird TC, Dolan CR, Stephens K, editors. GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle; 1993-.
    2003 May 20 [updated 2008 Aug 12].
    PMID: 20301534 [PubMed]Books & DocumentsFree textRelated citations

    4.

    Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism.

    Xu S, Han JC, Morales A, Menzie CM, Williams K, Fan YS.

    Cytogenet Genome Res. 2008;122(2):181-7. Epub 2008 Dec 18. Erratum in: Cytogenet Genome Res. 2009;124(1):112. PMID: 19096215 [PubMed - indexed for MEDLINE]Related citations

    5.

    WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH.

    Lennon PA, Scott DA, Lonsdorf D, Wargowski DS, Kirkpatrick S, Patel A, Cheung SW.

    Am J Med Genet A. 2006 Jun 1;140(11):1214-8.PMID: 16646034 [PubMed - indexed for MEDLINE]Related citations

    6.

    Congenital diaphragmatic hernia in WAGR syndrome.

    Scott DA, Cooper ML, Stankiewicz P, Patel A, Potocki L, Cheung SW.

    Am J Med Genet A. 2005 May 1;134(4):430-3. Review.PMID: 15779010 [PubMed - indexed for MEDLINE]Related citations

    7.

    Complete sex reversal in a WAGR syndrome patient.

    Le Caignec C, Delnatte C, Vermeesch JR, Boceno M, Joubert M, Lavenant F, David A, Rival JM.

    Am J Med Genet A. 2007 Nov 15;143A(22):2692-5.PMID: 17935232 [PubMed - indexed for MEDLINE]Related citations

    8.

    WAGR syndrome--a case report.

    Mahale A, Poornima V, Shrestha M.

    Nepal Med Coll J. 2007 Jun;9(2):138-40.PMID: 17899969 [PubMed - indexed for MEDLINE]Related citations

    9.

    Brain-derived neurotrophic factor and obesity in the WAGR syndrome.

    Han JC, Liu QR, Jones M, Levinn RL, Menzie CM, Jefferson-George KS, Adler-Wailes DC, Sanford EL, Lacbawan FL, Uhl GR, Rennert OM, Yanovski JA.

    N Engl J Med. 2008 Aug 28;359(9):918-27. Erratum in: N Engl J Med. 2008 Sep 25;359(13):1414. PMID: 18753648 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

    10.

    A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.

    Crolla JA, Cawdery JE, Oley CA, Young ID, Gray J, Fantes J, van Heyningen V.

    J Med Genet. 1997 Mar;34(3):207-12.PMID: 9132491 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

    11.

    Aniridia as part of a WAGR syndrome in a girl whose brother presented hypospadias.

    Lorda-Sanchez I, Sanz R, Diaz-Guillen MA, Fernandez-Toral J, Heine-Suñer D, Rodriguez De Alba M, Gonzalez-Gonzalez C, Trujillo MJ, Ramos C, Rodriguez De Cordoba S, Ayuso C.

    Genet Couns. 2002;13(2):171-7.PMID: 12150218 [PubMed - indexed for MEDLINE]Related citations

    12.

    Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia.

    Crolla JA, van Heyningen V.

    Am J Hum Genet. 2002 Nov;71(5):1138-49. Epub 2002 Oct 17.PMID: 12386836 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

    13.

    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 1;134(4):422-5.PMID: 15779023 [PubMed - indexed for MEDLINE]Related citations

    14.

    Construction of a natural panel of 11p11.2 deletions and further delineation of the critical region involved in Potocki-Shaffer syndrome.

    Wakui K, Gregato G, Ballif BC, Glotzbach CD, Bailey KA, Kuo PL, Sue WC, Sheffield LJ, Irons M, Gomez EG, Hecht JT, Potocki L, Shaffer LG.

    Eur J Hum Genet. 2005 May;13(5):528-40.PMID: 15852040 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

    15.

    Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene.

    Drechsler M, Meijers-Heijboer EJ, Schneider S, Schurich B, Grond-Ginsbach C, Tariverdian G, Kantner G, Blankenagel A, Kaps D, Schroeder-Kurth T, et al.

    Hum Genet. 1994 Oct;94(4):331-8.PMID: 7927324 [PubMed - indexed for MEDLINE]Related citations

    16.

    [WAGR syndrome: a case report]

    Moreno García M, Sánchez del Pozo J, Fernández Martínez FJ, Moreno-Izquierdo A, Barreiro Miranda E.

    An Esp Pediatr. 1998 Oct;49(4):381-7. Spanish. PMID: 9859552 [PubMed - indexed for MEDLINE]Related citations

    17.

    [Two neonates with congenital aniridia: the necessity of genetic investigation]

    van Os E, Niemarkt HJ, Verreussel MJ, Cruysberg JR, Bok LA, Spruijt L.

    Ned Tijdschr Geneeskd. 2008 Mar 8;152(10):569-73. Dutch. PMID: 18402324 [PubMed - indexed for MEDLINE]Related citations

    18.

    Familial case of Potocki-Shaffer syndrome associated with microdeletion of EXT2 and ALX4.

    Hall CR, Wu Y, Shaffer LG, Hecht JT.

    Clin Genet. 2001 Nov;60(5):356-9.PMID: 11903336 [PubMed - indexed for MEDLINE]Related citations

    19.

    Clinical, cytogenetic and molecular characterization of a patient with combined succinic semialdehyde dehydrogenase deficiency and incomplete WAGR syndrome with obesity.

    Jung R, Rauch A, Salomons GS, Verhoeven NM, Jakobs C, Michael Gibson K, Lachmann E, Sass JO, Trautmann U, Zweier C, Staatz G, Knerr I.

    Mol Genet Metab. 2006 Jul;88(3):256-60. Epub 2006 Mar 20.PMID: 16545979 [PubMed - indexed for MEDLINE]Related citations

    20.

    Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization.

    Fantes JA, Bickmore WA, Fletcher JM, Ballesta F, Hanson IM, van Heyningen V.

    Am J Hum Genet. 1992 Dec;51(6):1286-94.PMID: 1334370 [PubMed - indexed for MEDLINE]Free PMC ArticleFree textRelated citations

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