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Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease

✍ Scribed by Matthew G. Sampson; Curtis R. Coughlin II; Paige Kaplan; Laura K. Conlin; Kevin E.C. Meyers; Elaine H. Zackai; Nancy B. Spinner; Lawrence Copelovitch


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
144 KB
Volume
152A
Category
Article
ISSN
1552-4825

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