Identification of critical regions for clinical features of distal 10q deletion syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2008.01115.x/fullpdf
Reference29 articles.
1. Deletion of the distal long arm of chromosome 10: is there a characteristic phenotype? A report of 15 de novo and familial cases;Irving;Am J Med Genet A,2003
2. Interstitial deletion del(10)(q25.2q25.3 approximately 26.11) - case report and review of the literature;Kehrer-Sawatzki;Prenat Diagn,2005
3. A case of interstitial deletion of 10q25.2-q26.1;Rooney;J Med Genet,1989
4. Partial monosomy of distal 10q: three new cases and a review;Waggoner;Am J Med Genet,1999
5. Adult with an interstitial deletion of chromosome 10 [del(10)(q25.1q25.3)]: overlap with Coffin-Lowry syndrome;McCandless;Am J Med Genet,2000
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