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Teenager with uterine didelphys, absent kidney and 22q11.2 deletion

✍ Scribed by Angela Scheuerle

Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 35 KB
Volume: 146A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.32224

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## Abstract ## BACKGROUND: Children with 22q11.2 deletion syndrome (22q11.2DS) have a wide range of clinical features. __TBX1__ has been proposed as a candidate gene for some of the features in this condition. Polymorphisms in the nondeleted __TBX1,__ which may affect the function of the sole __TB