BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 17935232)

  • 1. 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; 143A(22):2692-5. PubMed ID: 17935232
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 134(4):430-3. PubMed ID: 15779010
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Narrowing of the responsible region for severe developmental delay and autistic behaviors in WAGR syndrome down to 1.6 Mb including PAX6, WT1, and PRRG4.
    Yamamoto T; Togawa M; Shimada S; Sangu N; Shimojima K; Okamoto N
    Am J Med Genet A; 2014 Mar; 164A(3):634-8. PubMed ID: 24357251
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. WAGR syndrome--a case report.
    Mahale A; Poornima V; Shrestha M
    Nepal Med Coll J; 2007 Jun; 9(2):138-40. PubMed ID: 17899969
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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. PubMed ID: 12386836
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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. PubMed ID: 12150218
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical utility gene card for: WAGR syndrome.
    Clericuzio C; Hingorani M; Crolla JA; van Heyningen V; Verloes A
    Eur J Hum Genet; 2011 Apr; 19(4):. PubMed ID: 21224893
    [No Abstract]   [Full Text] [Related]  

  • 9. [WAGR syndrome by heterozygous deletion of the WT1 gene. Pediatric case report].
    Galvis-Blanco SJ; Arias-Flórez JS; Contreras-García GA
    Arch Argent Pediatr; 2019 Oct; 117(5):e505-e508. PubMed ID: 31560501
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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; 152(10):569-73. PubMed ID: 18402324
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mosaic deletion 11p13 in a child with dopamine beta-hydroxylase deficiency--case report and review of the literature.
    Erez A; Li J; Geraghty MT; Ben-Shachar S; Cooper ML; Mensing DE; Vonalt KD; Ou Z; Pursley AN; Chinault AC; Patel A; Cheung SW; Sahoo T
    Am J Med Genet A; 2010 Mar; 152A(3):732-6. PubMed ID: 20186791
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis.
    Melo KF; Martin RM; Costa EM; Carvalho FM; Jorge AA; Arnhold IJ; Mendonca BB
    J Clin Endocrinol Metab; 2002 Jun; 87(6):2500-5. PubMed ID: 12050205
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 gene.
    Köhler B; Schumacher V; Schulte-Overberg U; Biewald W; Lennert T; l'Allemand D; Royer-Pokora B; Grüters A
    Pediatr Res; 1999 Feb; 45(2):187-90. PubMed ID: 10022588
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Small glomeruli in WAGR (Wilms Tumor, Aniridia, Genitourinary Anomalies and Mental Retardation) syndrome.
    Dahan K; Kamal M; Noël LH; Jeanpierre C; Gubler MC; Brousse N; Mariaud de Serre NP
    Am J Kidney Dis; 2007 Jun; 49(6):793-800. PubMed ID: 17533022
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Aniridia-Wilms tumor association].
    Imaizumi K
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):327-8. PubMed ID: 11057248
    [No Abstract]   [Full Text] [Related]  

  • 16. [WAGR syndrome].
    Kaneko Y
    Nihon Rinsho; 2006 Sep; Suppl 3():605-8. PubMed ID: 17022619
    [No Abstract]   [Full Text] [Related]  

  • 17. Prediction by FISH analysis of the occurrence of Wilms tumor in aniridia patients.
    Muto R; Yamamori S; Ohashi H; Osawa M
    Am J Med Genet; 2002 Apr; 108(4):285-9. PubMed ID: 11920832
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Genetics of congenital aniridia].
    Neuhaus C; Betz C; Bergmann C; Bolz HJ
    Ophthalmologe; 2014 Dec; 111(12):1157-63. PubMed ID: 25475187
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 140(11):1214-8. PubMed ID: 16646034
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.