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Items: 1 to 20 of 98

1.

WAGR syndrome with tetralogy of Fallot and hydrocephalus.

Demir HA, Varan A, Utine EG, Aktaş D, Oğuz B, Rama D, Büyükpamukçu M.

J Pediatr Hematol Oncol. 2011 May;33(4):e174-5. doi: 10.1097/MPH.0b013e3182114e0e.

PMID:
21364466
2.

[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. Spanish.

PMID:
9859552
3.

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.

PMID:
12150218
4.

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 1;140(11):1214-8.

PMID:
16646034
5.

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. Epub 2006 Mar 20.

PMID:
16545979
6.

Third case of WAGR syndrome with severe obesity and constitutional deletion of chromosome (11)(p12p14).

Gül D, Oğur G, Tunca Y, Ozcan O.

Am J Med Genet. 2002 Jan 1;107(1):70-1. No abstract available.

PMID:
11807873
7.

[Association between WAGR syndrome and diaphragmatic hernia].

Martín Campagne E, Guerrero Fernández J, Gracia Bouthelier R, Tovar Larrucea JA.

An Pediatr (Barc). 2006 Dec;65(6):616-8. Spanish.

8.

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. doi: 10.1159/000172086. Epub 2008 Dec 18. Erratum in: Cytogenet Genome Res. 2009;124(1):112.

PMID:
19096215
9.

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 15;53(20):4757-60.

10.

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. Review.

PMID:
16199712
11.

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.

PMID:
17533022
12.

Focal segmental glomerulosclerosis in solitary kidney in WAGR syndrome.

Merta M, Reiterová J, Krkavcová M, Rysavá R, Kmentová D, Tesar V.

Prague Med Rep. 2004;105(1):69-73.

PMID:
15354948
13.

HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.

Porteous DJ, Bickmore W, Christie S, Boyd PA, Cranston G, Fletcher JM, Gosden JR, Rout D, Seawright A, Simola KO, et al.

Proc Natl Acad Sci U S A. 1987 Aug;84(15):5355-9.

14.

The distal region of 11p13 and associated genetic diseases.

Mannens M, Hoovers JM, Bleeker-Wagemakers EM, Redeker E, Bliek J, Overbeeke-Melkert M, Saunders G, Williams B, van Heyningen V, Junien C, et al.

Genomics. 1991 Oct;11(2):284-93.

PMID:
1769647
15.

A deletion map of the WAGR region on chromosome 11.

Gessler M, Thomas GH, Couillin P, Junien C, McGillivray BC, Hayden M, Jaschek G, Bruns GA.

Am J Hum Genet. 1989 Apr;44(4):486-95.

16.

[Hereditary renal tumors: Wilms' tumor--congenital anomalies' syndrome].

Tsuchida Y, Yokomori K, Choi SH.

Nihon Rinsho. 1995 Nov;53(11):2742-8. Review. Japanese.

PMID:
8538037
17.

A 1.7-Mb YAC contig around the human BDNF gene (11p13): integration of the physical, genetic, and cytogenetic maps in relation to WAGR syndrome.

Rosier MF, Goguel AF, Martin A, Le Paslier D, Couillin P, Houlgatte R, Bernheim A, Auffray C, Devignes MD.

Genomics. 1994 Nov 1;24(1):69-77.

PMID:
7896291
18.

[WAGR syndrome, Wilms' tumor, aniridia, gonadoblastoma, mental retardation: a review apropos of 2 cases].

Mochon MC, Blanc JF, Plauchu H, Philip T.

Pediatrie. 1987;42(4):249-52. French.

PMID:
2823214
19.

Hitch-hiking from HRAS1 to the WAGR locus with CMGT markers.

Bickmore W, Christie S, van Heyningen V, Hastie ND, Porteous DJ.

Nucleic Acids Res. 1988 Jan 11;16(1):51-60.

20.

Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells.

Reeve AE, Sih SA, Raizis AM, Feinberg AP.

Mol Cell Biol. 1989 Apr;9(4):1799-803.

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