BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 37742703)

  • 21. The genetic architecture of aniridia and Gillespie syndrome.
    Hall HN; Williamson KA; FitzPatrick DR
    Hum Genet; 2019 Sep; 138(8-9):881-898. PubMed ID: 30242502
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. Obesity: a new feature of WAGR (del 11p) syndrome.
    Marlin S; Couet D; Lacombe D; Cessans C; Bonneau D
    Clin Dysmorphol; 1994 Jul; 3(3):255-7. PubMed ID: 7526938
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. A rare case of an isolated PAX6 mutation, aniridia, and Wilms tumor.
    Lind KT; Cost NG; Zegar K; Kuldanek SA; Enzenauer RW; Schneider KW
    Ophthalmic Genet; 2021 Apr; 42(2):216-217. PubMed ID: 33300417
    [No Abstract]   [Full Text] [Related]  

  • 27. 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]  

  • 28. Bilateral aniridia and congenital ureteral valve: Role of genetic testing.
    Shields LBE; Peppas DS; Rosenberg E
    Mol Genet Genomic Med; 2020 Apr; 8(4):e1183. PubMed ID: 32056389
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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. PubMed ID: 15702131
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Preferentially Paternal Origin of De Novo 11p13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome.
    Vasilyeva TA; Marakhonov AV; Sukhanova NV; Kutsev SI; Zinchenko RA
    Genes (Basel); 2020 Jul; 11(7):. PubMed ID: 32708836
    [TBL] [Abstract][Full Text] [Related]  

  • 31. WAGR syndrome: a clinical review of 54 cases.
    Fischbach BV; Trout KL; Lewis J; Luis CA; Sika M
    Pediatrics; 2005 Oct; 116(4):984-8. PubMed ID: 16199712
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Billateral polycystic kidneys in a girl with WAGR syndrome.
    Gucev Z; Muratovska O; Laban N; Misevska L; Jancevska A; Crolla J; Tasic V
    Indian J Pediatr; 2011 Oct; 78(10):1290-2. PubMed ID: 21660403
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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. PubMed ID: 16545979
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977 kb deletion in the 11p13 region.
    Vasilyeva TA; Marakhonov AV; Minzhenkova ME; Markova ZG; Petrova NV; Sukhanova NV; Koshkin PA; Pyankov DV; Kanivets IV; Korostelev SA; Krynskaya IA; Shilova NV; Kutsev SI; Kadyshev VV; Zinchenko RA
    BMC Med Genomics; 2020 Sep; 13(Suppl 8):130. PubMed ID: 32948199
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30-year SIOP-RTSG experience.
    Hol JA; Jongmans MCJ; Sudour-Bonnange H; Ramírez-Villar GL; Chowdhury T; Rechnitzer C; Pal N; Schleiermacher G; Karow A; Kuiper RP; de Camargo B; Avcin S; Redzic D; Wachtel A; Segers H; Vujanic GM; van Tinteren H; Bergeron C; Pritchard-Jones K; Graf N; van den Heuvel-Eibrink MM;
    Cancer; 2021 Feb; 127(4):628-638. PubMed ID: 33146894
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutation in the PAX6 gene in twenty patients with aniridia.
    Chao LY; Huff V; Strong LC; Saunders GF
    Hum Mutat; 2000; 15(4):332-9. PubMed ID: 10737978
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [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]  

    [Previous]   [Next]    [New Search]
    of 7.