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Items: 1 to 20 of 92

1.

Obesity and WAGR syndrome.

Tiberio G, Digilio MC, Giannotti A.

Clin Dysmorphol. 2000 Jan;9(1):63-4.

PMID:
10649802
2.

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
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.

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
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.

Bilateral preaxial polydactyly in a WAGR syndrome patient.

Manoukian S, Crolla JA, Mammoliti PM, Testi MA, Zanini R, Carpanelli ML, Piozzi E, Sozzi G, De Vecchi G, Terenziani M, Spreafico F, Collini P, Radice P, Perotti D.

Am J Med Genet A. 2005 May 1;134(4):426-9.

PMID:
15742368
7.

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
8.

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
9.

Morbid obesity and hyperphagia in the WAGR syndrome.

Amor DJ.

Clin Dysmorphol. 2002 Jan;11(1):73-4.

PMID:
11822711
10.

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
11.

The modifier effect of the BDNF gene in the phenotype of the WAGRO syndrome.

Rodríguez-López R, Pérez JM, Balsera AM, Rodríguez GG, Moreno TH, García de Cáceres M, Serrano MG, Freijo FC, Ruiz JR, Angueira FB, Pérez PM, Estévez MN, Gómez EG.

Gene. 2013 Mar 10;516(2):285-90. doi: 10.1016/j.gene.2012.11.073. Epub 2012 Dec 21.

PMID:
23266638
12.

Brain-derived neurotrophic factor and obesity in the WAGR syndrome.

Han JC, Liu QR, Jones M, Levinn RL, Menzie CM, Jefferson-George KS, Adler-Wailes DC, Sanford EL, Lacbawan FL, Uhl GR, Rennert OM, Yanovski JA.

N Engl J Med. 2008 Aug 28;359(9):918-27. doi: 10.1056/NEJMoa0801119. Erratum in: N Engl J Med. 2008 Sep 25;359(13):1414.

13.

WAGR complex.

Sarin YK, Mathur P, Goyal RB, Jhamaria VN, Sharma R, Shekhawat NS.

Indian Pediatr. 1993 May;30(5):662-4. No abstract available.

PMID:
8282394
14.

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.

15.

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 1;134(4):422-5.

PMID:
15779023
16.

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
17.

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
18.

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
19.

[Typical WAGR syndrome in a case].

Zheng XS, Han N, Kuang L.

Zhonghua Er Ke Za Zhi. 2013 Mar;51(3):237-9. Chinese. No abstract available.

PMID:
23751590
20.

WAGR syndrome and multiple exostoses in a patient with del(11)(p11.2p14.2).

McGaughran JM, Ward HB, Evans DG.

J Med Genet. 1995 Oct;32(10):823-4. No abstract available.

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