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Items: 1 to 20 of 185

1.

Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)].

Moore JW, Hyman S, Antonarakis SE, Mules EH, Thomas GH.

Hum Genet. 1986 Apr;72(4):297-302.

PMID:
3754537
2.

Regional mapping of catalase and Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305----p1306.

Narahara K, Kikkawa K, Kimira S, Kimoto H, Ogata M, Kasai R, Hamawaki M, Matsuoka K.

Hum Genet. 1984;66(2-3):181-5.

PMID:
6325323
3.

The E7-associated cell-surface antigen: a marker for the 11p13 chromosomal deletion associated with aniridia-Wilms tumor.

Scoggin CH, Fisher JH, Shoemaker SA, Morse H, Leigh T, Riccardi VM.

Am J Hum Genet. 1985 Sep;37(5):883-9.

4.

Familial aniridia and translocation t(4;11)(q22;p13) without Wilms' tumor.

Simola KO, Knuutila S, Kaitila I, Pirkola A, Pohja P.

Hum Genet. 1983;63(2):158-61.

PMID:
6301974
5.

The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.

Glaser T, Lewis WH, Bruns GA, Watkins PC, Rogler CE, Shows TB, Powers VE, Willard HF, Goguen JM, Simola KO, et al.

Nature. 1986 Jun 26-Jul 2;321(6073):882-7.

PMID:
3014343
6.

Aniridia-Wilms' tumor association: evidence for specific deletion of 11p13.

Francke U, Holmes LB, Atkins L, Riccardi VM.

Cytogenet Cell Genet. 1979;24(3):185-92.

PMID:
225131
8.

Cloning of breakpoints of a chromosome translocation identifies the AN2 locus.

Gessler M, Simola KO, Bruns GA.

Science. 1989 Jun 30;244(4912):1575-8.

PMID:
2544995
9.

Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci.

Davis LM, Stallard R, Thomas GH, Couillin P, Junien C, Nowak NJ, Shows TB.

Science. 1988 Aug 12;241(4867):840-2.

PMID:
2841760
10.

Translocation t(5;11)(q13.1;p13) associated with familial isolated aniridia.

Pettenati MJ, Weaver RG, Burton BK.

Am J Med Genet. 1989 Oct;34(2):230-2.

PMID:
2817003
11.

De novo chromosome translocation t (2; 11) (p25.1; p13) in a patient with aniridia and genitourinary abnormalities.

Hung HM, Lin SC, Su PH, Chen JY.

Acta Paediatr Taiwan. 2003 Mar-Apr;44(2):101-3.

PMID:
12845852
12.

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.

13.

High-resolution studies in patients with aniridia-Wilms tumor association, Wilms tumor or related congenital abnormalities.

Nakagome Y, Ise T, Sakurai M, Nakajo T, Okamoto E, Takano T, Nakahori Y, Tsuchida Y, Nagahara N, Takada Y, et al.

Hum Genet. 1984;67(3):245-8.

PMID:
6088386
14.

Structural aberrations of the long arm of chromosome no. 22. Report fo a family with translocation t(11;22) (q25;q11).

Fu W, Borgaonkar DS, Ladewig PP, Weaver J, Pomerance HH.

Clin Genet. 1976 Dec;10(6):329-36.

PMID:
991443
15.

Trisomy 4p in four relatives: variability and lack of distinctive features in phenotypic expression.

Reynolds JF, Shires MA, Wyandt HE, Kelly TE.

Clin Genet. 1983 Nov;24(5):365-74.

PMID:
6418421
16.

Prediction by FISH analysis of the occurrence of Wilms tumor in aniridia patients.

Muto R, Yamamori S, Ohashi H, Osawa M.

Am J Med Genet. 2002 Apr 1;108(4):285-9.

PMID:
11920832
17.

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
18.

Two distinctive classic genetic syndromes, 22q11.2 deletion syndrome and Angelman syndrome, occurring within the same family.

Kosaki R, Migita O, Takahashi T, Kosaki K.

Am J Med Genet A. 2009 Feb 15;149A(4):702-5. doi: 10.1002/ajmg.a.32666.

PMID:
19288551
19.

Chromosome abnormalities involving 11p13 and low erythrocyte catalase activity.

Niikawa N, Fukushima Y, Taniguchi N, Iizuka S, Kajii T.

Hum Genet. 1982;60(4):373-5.

PMID:
7106775
20.

Repeated unbalanced offspring due to a familial translocation involving chromosomes 5 and 6.

Groen SE, Drewes JG, de Boer EG, Hoovers JM, Hennekam RC.

Am J Med Genet. 1998 Dec 28;80(5):448-53.

PMID:
9880207

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