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3. A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X. Heathcott RW; Morison IM; Gubler MC; Corbett R; Reeve AE Hum Mutat; 2002 Apr; 19(4):462. PubMed ID: 11933209 [TBL] [Abstract][Full Text] [Related]
4. Case report: WT1 exon 6 truncation mutation and ambiguous genitalia in a patient with Denys-Drash syndrome. Chiang PW; Aliaga S; Travers S; Spector E; Tsai AC Curr Opin Pediatr; 2008 Feb; 20(1):103-6. PubMed ID: 18197048 [TBL] [Abstract][Full Text] [Related]
5. Effects of Denys-Drash syndrome point mutations on the DNA binding activity of the Wilms' tumor suppressor protein WT1. Borel F; Barilla KC; Hamilton TB; Iskandar M; Romaniuk PJ Biochemistry; 1996 Sep; 35(37):12070-6. PubMed ID: 8810912 [TBL] [Abstract][Full Text] [Related]
6. A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys-Drash syndrome. da Silva TE; Nishi MY; Costa EM; Martin RM; Carvalho FM; Mendonca BB; Domenice S Pediatr Nephrol; 2011 Aug; 26(8):1311-5. PubMed ID: 21559934 [TBL] [Abstract][Full Text] [Related]
7. Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children. Yue Z; Pei Y; Sun L; Huang W; Huang H; Hu B; Yang J; Jiang X; Mo Y; Chen S; Lai KN; Wang Y Ren Fail; 2011; 33(9):910-4. PubMed ID: 21851196 [TBL] [Abstract][Full Text] [Related]
8. A WT1 exon 1 mutation in a child diagnosed with Denys-Drash syndrome. Little S; Hanks S; King-Underwood L; Picton S; Cullinane C; Rapley E; Rahman N; Pritchard-Jones K Pediatr Nephrol; 2005 Jan; 20(1):81-5. PubMed ID: 15503171 [TBL] [Abstract][Full Text] [Related]
9. A novel WT1 gene mutation in a patient with Wilms' tumor and 46, XY gonadal dysgenesis. Lee DG; Han DH; Park KH; Baek M Eur J Pediatr; 2011 Aug; 170(8):1079-82. PubMed ID: 21384108 [TBL] [Abstract][Full Text] [Related]
11. Denys-Drash syndrome with neonatal renal failure in monozygotic twins due to c.1097G>A mutation in the WT1 gene. Furtado LV; Pysher T; Opitz J; Lamb R; Comstock J; Batish S; Mauch T; Nelson R; Zhou H Fetal Pediatr Pathol; 2011; 30(4):266-72. PubMed ID: 21434831 [TBL] [Abstract][Full Text] [Related]
12. WT1 Haploinsufficiency Supports Milder Renal Manifestation in Two Patients with Denys-Drash Syndrome. Guaragna MS; Ribeiro de Andrade JG; de Freitas Carli B; Belangero VM; Maciel-Guerra AT; Guerra-Júnior G; de Mello MP Sex Dev; 2017; 11(1):34-39. PubMed ID: 28081536 [TBL] [Abstract][Full Text] [Related]
13. [A case of Denys-Drash syndrome with prophylactic bilateral nephrectomy]. Yamamoto K; Santo Y; Satomura K Nihon Jinzo Gakkai Shi; 2003; 45(1):42-6. PubMed ID: 12680320 [TBL] [Abstract][Full Text] [Related]
14. Prophylactic bilateral nephrectomies in two paediatric patients with missense mutations in the WT1 gene. Hu M; Zhang GY; Arbuckle S; Graf N; Shun A; Silink M; Lewis D; Alexander SI Nephrol Dial Transplant; 2004 Jan; 19(1):223-6. PubMed ID: 14671061 [TBL] [Abstract][Full Text] [Related]
15. A novel WT1 missense mutation presenting with Denys-Drash syndrome and cortical atrophy. Schumacher V; Thumfart J; Drechsler M; Essayie M; Royer-Pokora B; Querfeld U; Müller D Nephrol Dial Transplant; 2006 Feb; 21(2):518-21. PubMed ID: 16303781 [No Abstract] [Full Text] [Related]
16. Novel WT1 mutation (C388Y) in a female child with Denys-Drash syndrome. Swiatecka-Urban A; Mokrzycki MH; Kaskel F; Da Silva F; Denamur E Pediatr Nephrol; 2001 Aug; 16(8):627-30. PubMed ID: 11519891 [TBL] [Abstract][Full Text] [Related]
17. Murine Denys-Drash syndrome: evidence of podocyte de-differentiation and systemic mediation of glomerulosclerosis. Patek CE; Fleming S; Miles CG; Bellamy CO; Ladomery M; Spraggon L; Mullins J; Hastie ND; Hooper ML Hum Mol Genet; 2003 Sep; 12(18):2379-94. PubMed ID: 12915483 [TBL] [Abstract][Full Text] [Related]
18. [Clinical and pathological features of Denys-Drash syndrome: report of 3 cases]. Wang HY; Sun LZ; Yue ZH; Yang J; Jiang XY; Mo Y Zhonghua Er Ke Za Zhi; 2012 Nov; 50(11):855-8. PubMed ID: 23302619 [TBL] [Abstract][Full Text] [Related]