9q22 Deletion - First Familial Case

9q22 Deletion - First Familial Case

<p>Abstract</p> <p>Background</p> <p>Only 29 cases of constitutional 9q22 deletions have been published and all have been sporadic. Most associate with Gorlin syndrome or nevoid basal cell carcinoma syndrome (NBCCS, MIM #109400) due to haploinsufficiency of the <it&g...

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Bibliographic Details
Main Authors: Yamamoto Toshiyuki, Shimojima Keiko, Miikkulainen Taina, Sipponen Marjatta, Peippo Maarit, Siggberg Linda, Ignatius Jaakko, Knuutila Sakari
Format: Article
Language:English
Published: BMC 2011-06-01
Series:Orphanet Journal of Rare Diseases
Online Access:http://www.ojrd.com/content/6/1/45

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http://www.ojrd.com/content/6/1/45

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