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Items: 1 to 20 of 97

1.

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
2.

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
3.

[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
4.

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
5.

[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.

6.

WAGR syndrome--a case report.

Starcević M, Mataija M.

Acta Clin Croat. 2009 Sep;48(4):455-9.

PMID:
20405644
7.

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
8.

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
9.

WAGR syndrome: is the 'R' always justified?

Termine C, Parigi G, Rossi M, Romano P, Balottin U.

Clin Dysmorphol. 2007 Jan;16(1):69-70.

PMID:
17159522
10.

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
11.

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.

PMID:
8817218
12.

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
13.

Characterization of an evolutionarily conserved metallophosphoesterase that is expressed in the fetal brain and associated with the WAGR syndrome.

Tyagi R, Shenoy AR, Visweswariah SS.

J Biol Chem. 2009 Feb 20;284(8):5217-28. doi: 10.1074/jbc.M805996200. Epub 2008 Nov 12.

14.

Wilm's tumour with WAGR complex.

Mathur P, Khamesera HL, Pendse AK, Chittora R, Porewal KK.

Indian J Cancer. 1996 Sep;33(3):136-8.

PMID:
9055487
15.

WAGR syndrome--a case report.

Mahale A, Poornima V, Shrestha M.

Nepal Med Coll J. 2007 Jun;9(2):138-40.

PMID:
17899969
16.

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
17.

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. doi: 10.1002/ajmg.a.36325. Epub 2013 Dec 19.

PMID:
24357251
18.

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.

PMID:
7526938
19.

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 28;289(13):8767-80. doi: 10.1074/jbc.M113.530816. Epub 2014 Feb 11.

20.

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 Nov-Dec;49(10):2700-10. doi: 10.1016/j.cortex.2013.02.009. Epub 2013 Feb 19.

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