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-Reference-Cited by-同舟云学术

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

Published:2007-10 Issue:4 Volume:16 Page:231-239
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Courtens Winnie,Wauters Jan,Wojciechowski Marek,Reyniers Edwin,Scheers Stefan,van Luijk Rob,Rooms Liesbeth,Kooy Frank,Wuyts Wim

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Reference42 articles.

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2. Partial trisomy 20q in a newborn with dextrocardia;Addor;Genet Couns,2002

3. Subtelomeric rearrangements detected in patients with idiopathic mental retardation;Anderlid;Am J Med Genet,2002

4. Trisomy 2q and monosomy 11q in the same individual: the importance of considering the deleted segment;Ardinger;Clin Genet,1987

5. Association of Jacobsen syndrome and bipolar affective disorder in a patient with a de novo 11q terminal deletion;Böhm;Am J Med Genet,2006

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3. Subtelomeric monosomy 11q and trisomy 16q in siblings and an unrelated child: Molecular characterization of two der(11)t(11;16);American Journal of Medical Genetics Part A;2011-08-10

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5. Interstitial 11q deletion derived from a maternal ins(4;11)(p14;q24.2q25): A patient report and review;American Journal of Medical Genetics Part A;2009-07