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Items: 1 to 20 of 30

1.

Mosaic deletion 11p13 in a child with dopamine beta-hydroxylase deficiency--case report and review of the literature.

Erez A, Li J, Geraghty MT, Ben-Shachar S, Cooper ML, Mensing DE, Vonalt KD, Ou Z, Pursley AN, Chinault AC, Patel A, Cheung SW, Sahoo T.

Am J Med Genet A. 2010 Mar;152A(3):732-6. doi: 10.1002/ajmg.a.33269. Review.

PMID:
20186791
2.

Ultra-high resolution array painting facilitates breakpoint sequencing.

Gribble SM, Kalaitzopoulos D, Burford DC, Prigmore E, Selzer RR, Ng BL, Matthews NS, Porter KM, Curley R, Lindsay SJ, Baptista J, Richmond TA, Carter NP.

J Med Genet. 2007 Jan;44(1):51-8. Epub 2006 Sep 13.

3.

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
4.

Paternal reciprocal translocation t(11;16)(p13;q24.3) in a Silver-Russel syndrome patient.

Rao VB, Lily K, Seema K, Ghosh K, Dipika M.

Ann Genet. 2003 Oct-Dec;46(4):475-8.

PMID:
14659785
5.

Unique insertional translocation in a childhood Wilms' tumor survivor detected when his daughter developed bilateral retinoblastoma.

Punnett A, Teshima I, Heon E, Budning A, Sutherland J, Gallie BL, Chan HS.

Am J Med Genet A. 2003 Jul 1;120A(1):105-9.

PMID:
12794701
6.

A submicroscopic deletion of 11p13 associated with the WAGR syndrome.

Nanclares GP, Martínez F, Bilbao JR, Navajas A, Martínez R, López-Arístegui MA, Castaño L.

Clin Genet. 2003 Apr;63(4):319-22. No abstract available.

PMID:
12702167
7.

Familial (11;21)(p13;q22)pat balanced reciprocal translocation in a female child with regression of milestones.

Ramadevi AR, Prabhakara K, Dutta U.

Ann Genet. 2002 Jan-Mar;45(1):13-5.

PMID:
11934384
8.

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
9.
10.

Chromosome number 11 and Wilms' tumor.

Slater RM, de Kraker J.

Cancer Genet Cytogenet. 1982 Mar;5(3):237-45.

PMID:
6279277
11.
12.

Genetics of Wilms' tumor.

Matsunaga E.

Hum Genet. 1981;57(3):231-46. Review. No abstract available.

PMID:
6265341
13.

Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex.

Junien C, Turleau C, de Grouchy J, Saïd R, Rethoré MO L, Tenconi R, Dufier JL.

Ann Genet. 1980;23(3):165-8.

PMID:
6252821
15.

Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literature.

Turleau C, de Grouchy J, Tournade MF, Gagnadoux MF, Junien C.

Clin Genet. 1984 Oct;26(4):356-62.

PMID:
6094051
16.

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
17.
18.
19.

Prenatal diagnosis of del(11)(p13p15).

Stern RJ, Hunter WS, Moross T, Gardner HA.

Prenat Diagn. 1988 Jan;8(1):1-6.

PMID:
3344262
20.

High resolution G-banding analysis in aniridia.

Hotta Y, Fujiki K, Ishida N, Kato K, Nakajima A, Takamatsu H.

Ophthalmic Paediatr Genet. 1987 Nov;8(3):145-50.

PMID:
2830569

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