BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 28398607)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. [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]  

  • 5. 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]  

  • 6. 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]  

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

  • 8. 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]  

  • 9. Sustained endocrine profiles of a girl with WAGR syndrome.
    Takada Y; Sakai Y; Matsushita Y; Ohkubo K; Koga Y; Akamine S; Torio M; Ishizaki Y; Sanefuji M; Torisu H; Shaw CA; Kagami M; Hara T; Ohga S
    BMC Med Genet; 2017 Oct; 18(1):117. PubMed ID: 29061165
    [TBL] [Abstract][Full Text] [Related]  

  • 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. PubMed ID: 9132491
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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. PubMed ID: 19096215
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Improving molecular diagnosis of aniridia and WAGR syndrome using customized targeted array-based CGH.
    Blanco-Kelly F; Palomares M; Vallespín E; Villaverde C; Martín-Arenas R; Vélez-Monsalve C; Lorda-Sánchez I; Nevado J; Trujillo-Tiebas MJ; Lapunzina P; Ayuso C; Corton M
    PLoS One; 2017; 12(2):e0172363. PubMed ID: 28231309
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association of brain-derived neurotrophic factor (BDNF) haploinsufficiency with lower adaptive behaviour and reduced cognitive functioning in WAGR/11p13 deletion syndrome.
    Han JC; Thurm A; Golden Williams C; Joseph LA; Zein WM; Brooks BP; Butman JA; Brady SM; Fuhr SR; Hicks MD; Huey AE; Hanish AE; Danley KM; Raygada MJ; Rennert OM; Martinowich K; Sharp SJ; Tsao JW; Swedo SE
    Cortex; 2013; 49(10):2700-10. PubMed ID: 23517654
    [TBL] [Abstract][Full Text] [Related]  

  • 15. WAGRO syndrome: a rare genetic condition associated with aniridia and additional ophthalmologic abnormalities.
    Ferreira MAT; Almeida Júnior IG; Kuratani DK; Rosa RFM; Gonzales JFO; Telles LEB; Ferrão YA; Zen PRG
    Arq Bras Oftalmol; 2019 May; 82(4):336-338. PubMed ID: 31116317
    [TBL] [Abstract][Full Text] [Related]  

  • 16. LMO2 gene deletions significantly worsen the prognosis of Wilms' tumor development in patients with WAGR syndrome.
    Marakhonov AV; Vasilyeva TA; Voskresenskaya AA; Sukhanova NV; Kadyshev VV; Kutsev SI; Zinchenko RA
    Hum Mol Genet; 2019 Oct; 28(19):3323-3326. PubMed ID: 31304537
    [TBL] [Abstract][Full Text] [Related]  

  • 17. LGR4/GPR48 inactivation leads to aniridia-genitourinary anomalies-mental retardation syndrome defects.
    Yi T; Weng J; Siwko S; Luo J; Li D; Liu M
    J Biol Chem; 2014 Mar; 289(13):8767-80. PubMed ID: 24519938
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Unusual Presentation in WAGR Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the Diseases.
    Wang Q; Zhang X; Qin T; Wang D; Lin X; Zhu Y; Tan H; Zhao L; Li J; Lin Z; Lin H; Chen W
    Genes (Basel); 2022 Aug; 13(8):. PubMed ID: 36011342
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.