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Items: 10

1.

A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and review.

Courtens W, Wauters J, Wojciechowski M, Reyniers E, Scheers S, van Luijk R, Rooms L, Kooy F, Wuyts W.

Clin Dysmorphol. 2007 Oct;16(4):231-9. Review.

PMID:
17786114
2.

Bipolar affective disorder associated with 11q24.2 disruption--a second report.

Reardon W, Dunlop A, Holden ST, Blennerhassett R.

Am J Med Genet A. 2007 Jun 15;143A(12):1263-7.

PMID:
17497717
3.

Association of Jacobsen syndrome and bipolar affective disorder in a patient with a de novo 11q terminal deletion.

Böhm D, Hoffmann K, Laccone F, Wilken B, Dechent P, Frahm J, Bartels I, Bohlander SK.

Am J Med Genet A. 2006 Feb 15;140(4):378-82.

PMID:
16419136
4.

Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)]: further evidence for phenotypic heterogeneity.

Giampietro PF, Babu D, Zabel CA, Silberman T, Zador I, DeBauche D, Ravnan JB, Dave BJ.

Am J Med Genet A. 2006 Feb 15;140(4):385-7. No abstract available.

PMID:
16411193
5.

Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1).

Zahn S, Ehrbrecht A, Bosse K, Kalscheuer V, Propping P, Schwanitz G, Albrecht B, Engels H.

Am J Med Genet A. 2005 Nov 15;139(1):19-24.

PMID:
16222663
6.

Deletion of 11q24.2-qter with agenesis of unilateral internal carotid artery and total anomalous pulmonary venous return.

Wu CH, Hwu WL, Wang JK, Young C, Peng SS, Kuo MF.

Am J Med Genet. 2001 Oct 15;103(3):245-8. No abstract available.

PMID:
11745999
7.

A case of discordant related abnormal karyotypes from chorionic villi and amniocytes.

Porter S, Wilson E, Tyler X, Warren R, ffrench-Constant C, Pearson J.

Prenat Diagn. 1999 Sep;19(9):887-90.

PMID:
10521853
8.

Micromegakaryocytes in a patient with partial deletion of the long arm of chromosome 11 [del(11)(q24.2qter)] and chronic thrombocytopenic purpura.

Gangarossa S, Mattina T, Romano V, Milana G, Mollica F, Schilirò G.

Am J Med Genet. 1996 Mar 15;62(2):120-3.

PMID:
8882392
9.

Deletion of (11)(q24.2) in a mother and daughter with similar phenotypes.

Neavel CB, Soukup S.

Am J Med Genet. 1994 Dec 1;53(4):321-4.

PMID:
7864040
10.

Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1.

Fryns JP, Kleczkowska A, Buttiens M, Marien P, van den Berghe H.

Clin Genet. 1986 Oct;30(4):255-60.

PMID:
3791674

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