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Items: 1 to 20 of 123

1.

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.

2.

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.

3.

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
4.

Gene for multiple exostoses (EXT2) maps to 11(p11.2p12) and is deleted in patients with a contiguous gene syndrome.

Ligon AH, Potocki L, Shaffer LG, Stickens D, Evans GA.

Am J Med Genet. 1998 Feb 17;75(5):538-40. No abstract available.

PMID:
9489802
5.

[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
6.

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
7.

Multiple exostoses in a patient with t(8;11)(q24.11;p15.5).

Ogle RF, Dalzell P, Turner G, Wass D, Yip MY.

J Med Genet. 1991 Dec;28(12):881-3.

9.

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
10.

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
11.

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
12.

A case of atypical WAGR syndrome with anterior segment anomaly and microphthalmos.

Kawase E, Tanaka K, Honna T, Azuma N.

Arch Ophthalmol. 2001 Dec;119(12):1855-6. No abstract available.

PMID:
11735802
13.

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
14.

Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion.

Wuyts W, Roland D, Lüdecke HJ, Wauters J, Foulon M, Van Hul W, Van Maldergem L.

Am J Med Genet. 2002 Dec 15;113(4):326-32.

PMID:
12457403
15.

[Langer-Giedion syndrome and deletion in the long arm of chromosome 8].

Zaletaev DV, Kuleshov NP, Lur'e IV, Marincheva GS.

Genetika. 1987 May;23(5):907-12. Russian.

PMID:
3497842
16.

Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.

Bartsch O, Wuyts W, Van Hul W, Hecht JT, Meinecke P, Hogue D, Werner W, Zabel B, Hinkel GK, Powell CM, Shaffer LG, Willems PJ.

Am J Hum Genet. 1996 Apr;58(4):734-42.

17.

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
18.

WAGR syndrome with deletion of chromosome 11p11.2-13.

Pinna A, Carta A, Mannazzu MC, Dore S, Balata A, Carta F.

J AAPOS. 2004 Aug;8(4):396-7. No abstract available.

PMID:
15314606
19.

Obesity and WAGR syndrome.

Tiberio G, Digilio MC, Giannotti A.

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

PMID:
10649802
20.

[Localization of the gene for 4 hereditary multiple exostoses families].

Tang Y, Xia JH, Zhou JN, Li HJ, Wang DP, Dai HP, Long ZG, Tang BS, Huang L, Deng HX.

Yi Chuan Xue Bao. 1998;25(1):1-7. Chinese.

PMID:
9648398

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