132 related articles for article (PubMed ID: 21473084)
21. 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]
22. Characteristics and outcomes of children with the Wilms tumor-Aniridia syndrome: a report from the National Wilms Tumor Study Group.
Breslow NE; Norris R; Norkool PA; Kang T; Beckwith JB; Perlman EJ; Ritchey ML; Green DM; Nichols KE;
J Clin Oncol; 2003 Dec; 21(24):4579-85. PubMed ID: 14673045
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. [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. PubMed ID: 9859552
[TBL] [Abstract][Full Text] [Related]
26. An uncommon presentation of WAGR syndrome with persistent fetal vasculature.
Devaraj A; Shetty S; Patnaik N; Parida H; Pandurangan S
J AAPOS; 2023 Dec; 27(6):357-359. PubMed ID: 37742703
[TBL] [Abstract][Full Text] [Related]
27. Neuropsychological and neurophysiological features of WAGR syndrome: Detailed comprehensive evaluation of a patient with severe intellectual disability and autism spectrum disorder.
Nishizawa H; Motobayashi M; Akahane M; Wakui K; Kitazawa N; Inaba Y; Fukushima Y; Kosho T
Brain Dev; 2022 Mar; 44(3):229-233. PubMed ID: 34876316
[TBL] [Abstract][Full Text] [Related]
28. The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.
Glaser T; Lewis WH; Bruns GA; Watkins PC; Rogler CE; Shows TB; Powers VE; Willard HF; Goguen JM; Simola KO
Nature; 1986 Jun 26-Jul 2; 321(6073):882-7. PubMed ID: 3014343
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Complex Chromosomal Rearrangement Involving Chromosomes 10 and 11, Accompanied by Two Adjacent 11p14.1p13 and 11p13p12 Deletions, Identified in a Patient with WAGR Syndrome.
Marakhonov AV; Vasilyeva TA; Minzhenkova ME; Sukhanova NV; Sparber PA; Andreeva NA; Teleshova MV; Baybagisova FK; Shilova NV; Kutsev SI; Zinchenko RA
Int J Mol Sci; 2023 Nov; 24(23):. PubMed ID: 38069245
[TBL] [Abstract][Full Text] [Related]
31. [Hereditary renal tumors: Wilms' tumor--congenital anomalies' syndrome].
Tsuchida Y; Yokomori K; Choi SH
Nihon Rinsho; 1995 Nov; 53(11):2742-8. PubMed ID: 8538037
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Prenatal Diagnosis of WAGR Syndrome.
Tezcan B; Rich P; Bhide A
Case Rep Obstet Gynecol; 2015; 2015():928585. PubMed ID: 26605098
[TBL] [Abstract][Full Text] [Related]
34. Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors.
Kaneko Y; Homma C; Maseki N; Sakurai M; Hata J
Cancer Res; 1991 Nov; 51(21):5937-42. PubMed ID: 1657374
[TBL] [Abstract][Full Text] [Related]
35. [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]
36. Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutations.
Vasilyeva TA; Voskresenskaya AA; Käsmann-Kellner B; Khlebnikova OV; Pozdeyeva NA; Bayazutdinova GM; Kutsev SI; Ginter EK; Semina EV; Marakhonov AV; Zinchenko RA
Clin Genet; 2017 Dec; 92(6):639-644. PubMed ID: 28321846
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Altered trans-activational properties of a mutated WT1 gene product in a WAGR-associated Wilms' tumor.
Park S; Tomlinson G; Nisen P; Haber DA
Cancer Res; 1993 Oct; 53(20):4757-60. PubMed ID: 8402654
[TBL] [Abstract][Full Text] [Related]
39. Wilms' tumor and associated malformations; report of two cases with WAGR and Drash syndrome.
Ozbey H; Boneval C; Kapran Y; Aksöyek S; Salman T; Celik A
Eur J Pediatr Surg; 1996 Jun; 6(3):186-8. PubMed ID: 8817218
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
