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NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness

✍ Scribed by Kerry K. Brown; Fowzan S. Alkuraya; Michael Matos; Richard L. Robertson; Virginia E. Kimonis; Cynthia C. Morton

Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 215 KB
Volume: 149A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.32764

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