✦ LIBER ✦
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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